Canonical Allele Identifier: CA1207934351

Gene: SERPINC1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903869G>T , CM000663.2:g.173903869G>T	GRCh38
NC_000001.10:g.173873007G>T , CM000663.1:g.173873007G>T	GRCh37
NC_000001.9:g.172139630G>T	NCBI36
NG_012462.1:g.18510C>A , LRG_577:g.18510C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.*20C>A MANE Select	ENSP00000356671.3:n.*20C>A
ENST00000367698.3:c.*20C>A	ENSP00000356671.3:n.*20C>A
ENST00000617423.4:c.*20C>A	ENSP00000478688.1:n.*20C>A
NM_000488.3:c.*20C>A , LRG_577t1:c.*20C>A	NP_000479.1:n.*20C>A
XM_005245198.2:c.*20C>A	XP_005245255.1:n.*20C>A
NM_001365052.1:c.*20C>A	NP_001351981.1:n.*20C>A
NM_000488.4:c.*20C>A MANE Select	NP_000479.1:n.*20C>A
NM_001365052.2:c.*20C>A	NP_001351981.1:n.*20C>A
NM_001386302.1:c.*20C>A	NP_001373231.1:n.*20C>A
NM_001386303.1:c.*20C>A	NP_001373232.1:n.*20C>A
NM_001386304.1:c.*20C>A	NP_001373233.1:n.*20C>A
NM_001386305.1:c.*20C>A	NP_001373234.1:n.*20C>A
NM_001386306.1:c.*20C>A	NP_001373235.1:n.*20C>A