Canonical Allele Identifier: CA1207937100
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910047A= , CM000663.2:g.173910047A= GRCh38
NC_000001.10:g.173879185A= , CM000663.1:g.173879185A= GRCh37
NC_000001.9:g.172145808A= NCBI36
NG_012462.1:g.12332T= , LRG_577:g.12332T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-105T= MANE Select ENSP00000356671.3:n.763-105T=
ENST00000367698.3:c.763-105T= ENSP00000356671.3:n.763-105T=
ENST00000487183.1:n.414-105T=
ENST00000617423.4:c.559+1817T= ENSP00000478688.1:n.559+1817T=
NM_000488.3:c.763-105T= , LRG_577t1:c.763-105T= NP_000479.1:n.763-105T=
XM_005245198.2:c.619-105T= XP_005245255.1:n.619-105T=
NM_001365052.1:c.619-105T= NP_001351981.1:n.619-105T=
NM_000488.4:c.763-105T= MANE Select NP_000479.1:n.763-105T=
NM_001365052.2:c.619-105T= NP_001351981.1:n.619-105T=
NM_001386302.1:c.886-105T= NP_001373231.1:n.886-105T=
NM_001386303.1:c.844-105T= NP_001373232.1:n.844-105T=
NM_001386304.1:c.742-105T= NP_001373233.1:n.742-105T=
NM_001386305.1:c.763-162T= NP_001373234.1:n.763-162T=
NM_001386306.1:c.547-105T= NP_001373235.1:n.547-105T=
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