Canonical Allele Identifier: CA2649174491
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173911659G>T , CM000663.2:g.173911659G>T GRCh38
NC_000001.10:g.173880797G>T , CM000663.1:g.173880797G>T GRCh37
NC_000001.9:g.172147420G>T NCBI36
NG_012462.1:g.10720C>A , LRG_577:g.10720C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.624+140C>A MANE Select ENSP00000356671.3:n.624+140C>A
ENST00000367698.3:c.624+140C>A ENSP00000356671.3:n.624+140C>A
ENST00000487183.1:n.329+140C>A
ENST00000617423.4:c.559+205C>A ENSP00000478688.1:n.559+205C>A
NM_000488.3:c.624+140C>A , LRG_577t1:c.624+140C>A NP_000479.1:n.624+140C>A
XM_005245198.2:c.480+140C>A XP_005245255.1:n.480+140C>A
NM_001365052.1:c.480+140C>A NP_001351981.1:n.480+140C>A
NM_000488.4:c.624+140C>A MANE Select NP_000479.1:n.624+140C>A
NM_001365052.2:c.480+140C>A NP_001351981.1:n.480+140C>A
NM_001386302.1:c.624+140C>A NP_001373231.1:n.624+140C>A
NM_001386303.1:c.705+140C>A NP_001373232.1:n.705+140C>A
NM_001386304.1:c.624+140C>A NP_001373233.1:n.624+140C>A
NM_001386305.1:c.624+140C>A NP_001373234.1:n.624+140C>A
NM_001386306.1:c.409-768C>A NP_001373235.1:n.409-768C>A