Canonical Allele Identifier: CA343774822
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879077G>T (hg19) chr1:g.173909939G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909939G>T , CM000663.2:g.173909939G>T GRCh38
NC_000001.10:g.173879077G>T , CM000663.1:g.173879077G>T GRCh37
NC_000001.9:g.172145700G>T NCBI36
NG_012462.1:g.12440C>A , LRG_577:g.12440C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.766C>A MANE Select ENSP00000356671.3:p.Leu256Met
ENST00000367698.3:c.766C>A ENSP00000356671.3:p.Leu256Met
ENST00000487183.1:n.417C>A
ENST00000617423.4:c.559+1925C>A ENSP00000478688.1:n.559+1925C>A
NM_000488.3:c.766C>A , LRG_577t1:c.766C>A NP_000479.1:p.Leu256Met
XM_005245198.2:c.622C>A XP_005245255.1:p.Leu208Met
NM_001365052.1:c.622C>A NP_001351981.1:p.Leu208Met
NM_000488.4:c.766C>A MANE Select NP_000479.1:p.Leu256Met
NM_001365052.2:c.622C>A NP_001351981.1:p.Leu208Met
NM_001386302.1:c.889C>A NP_001373231.1:p.Leu297Met
NM_001386303.1:c.847C>A NP_001373232.1:p.Leu283Met
NM_001386304.1:c.745C>A NP_001373233.1:p.Leu249Met
NM_001386305.1:c.763-54C>A NP_001373234.1:n.763-54C>A
NM_001386306.1:c.550C>A NP_001373235.1:p.Leu184Met
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