Canonical Allele Identifier: CA343774356
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878948T>C (hg19) chr1:g.173909810T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909810T>C , CM000663.2:g.173909810T>C GRCh38
NC_000001.10:g.173878948T>C , CM000663.1:g.173878948T>C GRCh37
NC_000001.9:g.172145571T>C NCBI36
NG_012462.1:g.12569A>G , LRG_577:g.12569A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.895A>G MANE Select ENSP00000356671.3:p.Thr299Ala
ENST00000367698.3:c.895A>G ENSP00000356671.3:p.Thr299Ala
ENST00000487183.1:n.546A>G
ENST00000617423.4:c.559+2054A>G ENSP00000478688.1:n.559+2054A>G
NM_000488.3:c.895A>G , LRG_577t1:c.895A>G NP_000479.1:p.Thr299Ala
XM_005245198.2:c.751A>G XP_005245255.1:p.Thr251Ala
NM_001365052.1:c.751A>G NP_001351981.1:p.Thr251Ala
NM_000488.4:c.895A>G MANE Select NP_000479.1:p.Thr299Ala
NM_001365052.2:c.751A>G NP_001351981.1:p.Thr251Ala
NM_001386302.1:c.1018A>G NP_001373231.1:p.Thr340Ala
NM_001386303.1:c.976A>G NP_001373232.1:p.Thr326Ala
NM_001386304.1:c.874A>G NP_001373233.1:p.Thr292Ala
NM_001386305.1:c.838A>G NP_001373234.1:p.Thr280Ala
NM_001386306.1:c.679A>G NP_001373235.1:p.Thr227Ala
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