Canonical Allele Identifier: CA1149061144
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914934A= , CM000663.2:g.173914934A= GRCh38
NC_000001.10:g.173884072A= , CM000663.1:g.173884072A= GRCh37
NC_000001.9:g.172150695A= NCBI36
NG_012462.1:g.7445T= , LRG_577:g.7445T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.42-15T= MANE Select ENSP00000356671.3:n.42-15T=
ENST00000367698.3:c.42-15T= ENSP00000356671.3:n.42-15T=
ENST00000494024.1:n.268-15T=
ENST00000617423.4:c.42-15T= ENSP00000478688.1:n.42-15T=
NM_000488.3:c.42-15T= , LRG_577t1:c.42-15T= NP_000479.1:n.42-15T=
XM_005245198.2:c.-103-15T= XP_005245255.1:n.-103-15T=
NM_001365052.1:c.-103-15T= NP_001351981.1:n.-103-15T=
NM_000488.4:c.42-15T= MANE Select NP_000479.1:n.42-15T=
NM_001365052.2:c.-103-15T= NP_001351981.1:n.-103-15T=
NM_001386302.1:c.42-15T= NP_001373231.1:n.42-15T=
NM_001386303.1:c.123-15T= NP_001373232.1:n.123-15T=
NM_001386304.1:c.42-15T= NP_001373233.1:n.42-15T=
NM_001386305.1:c.42-15T= NP_001373234.1:n.42-15T=
NM_001386306.1:c.42-15T= NP_001373235.1:n.42-15T=