Canonical Allele Identifier: CA1207936984
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909756A= , CM000663.2:g.173909756A= GRCh38
NC_000001.10:g.173878894A= , CM000663.1:g.173878894A= GRCh37
NC_000001.9:g.172145517A= NCBI36
NG_012462.1:g.12623T= , LRG_577:g.12623T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.949T= MANE Select ENSP00000356671.3:p.Leu317=
ENST00000367698.3:c.949T= ENSP00000356671.3:p.Leu317=
ENST00000487183.1:n.600T=
ENST00000617423.4:c.559+2108T= ENSP00000478688.1:n.559+2108T=
NM_000488.3:c.949T= , LRG_577t1:c.949T= NP_000479.1:p.Leu317=
XM_005245198.2:c.805T= XP_005245255.1:p.Leu269=
NM_001365052.1:c.805T= NP_001351981.1:p.Leu269=
NM_000488.4:c.949T= MANE Select NP_000479.1:p.Leu317=
NM_001365052.2:c.805T= NP_001351981.1:p.Leu269=
NM_001386302.1:c.1072T= NP_001373231.1:p.Leu358=
NM_001386303.1:c.1030T= NP_001373232.1:p.Leu344=
NM_001386304.1:c.928T= NP_001373233.1:p.Leu310=
NM_001386305.1:c.892T= NP_001373234.1:p.Leu298=
NM_001386306.1:c.733T= NP_001373235.1:p.Leu245=