Canonical Allele Identifier: CA1207937073
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909990G= , CM000663.2:g.173909990G= GRCh38
NC_000001.10:g.173879128G= , CM000663.1:g.173879128G= GRCh37
NC_000001.9:g.172145751G= NCBI36
NG_012462.1:g.12389C= , LRG_577:g.12389C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-48C= MANE Select ENSP00000356671.3:n.763-48C=
ENST00000367698.3:c.763-48C= ENSP00000356671.3:n.763-48C=
ENST00000487183.1:n.414-48C=
ENST00000617423.4:c.559+1874C= ENSP00000478688.1:n.559+1874C=
NM_000488.3:c.763-48C= , LRG_577t1:c.763-48C= NP_000479.1:n.763-48C=
XM_005245198.2:c.619-48C= XP_005245255.1:n.619-48C=
NM_001365052.1:c.619-48C= NP_001351981.1:n.619-48C=
NM_000488.4:c.763-48C= MANE Select NP_000479.1:n.763-48C=
NM_001365052.2:c.619-48C= NP_001351981.1:n.619-48C=
NM_001386302.1:c.886-48C= NP_001373231.1:n.886-48C=
NM_001386303.1:c.844-48C= NP_001373232.1:n.844-48C=
NM_001386304.1:c.742-48C= NP_001373233.1:n.742-48C=
NM_001386305.1:c.763-105C= NP_001373234.1:n.763-105C=
NM_001386306.1:c.547-48C= NP_001373235.1:n.547-48C=