Canonical Allele Identifier: CA343774561
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909858T>C , CM000663.2:g.173909858T>C GRCh38
NC_000001.10:g.173878996T>C , CM000663.1:g.173878996T>C GRCh37
NC_000001.9:g.172145619T>C NCBI36
NG_012462.1:g.12521A>G , LRG_577:g.12521A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.847A>G MANE Select ENSP00000356671.3:p.Met283Val
ENST00000367698.3:c.847A>G ENSP00000356671.3:p.Met283Val
ENST00000487183.1:n.498A>G
ENST00000617423.4:c.559+2006A>G ENSP00000478688.1:n.559+2006A>G
NM_000488.3:c.847A>G , LRG_577t1:c.847A>G NP_000479.1:p.Met283Val
XM_005245198.2:c.703A>G XP_005245255.1:p.Met235Val
NM_001365052.1:c.703A>G NP_001351981.1:p.Met235Val
NM_000488.4:c.847A>G MANE Select NP_000479.1:p.Met283Val
NM_001365052.2:c.703A>G NP_001351981.1:p.Met235Val
NM_001386302.1:c.970A>G NP_001373231.1:p.Met324Val
NM_001386303.1:c.928A>G NP_001373232.1:p.Met310Val
NM_001386304.1:c.826A>G NP_001373233.1:p.Met276Val
NM_001386305.1:c.790A>G NP_001373234.1:p.Met264Val
NM_001386306.1:c.631A>G NP_001373235.1:p.Met211Val