Canonical Allele Identifier: CA343774096

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878885G>C (hg19) ; chr1:g.173909747G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909747G>C , CM000663.2:g.173909747G>C	GRCh38
NC_000001.10:g.173878885G>C , CM000663.1:g.173878885G>C	GRCh37
NC_000001.9:g.172145508G>C	NCBI36
NG_012462.1:g.12632C>G , LRG_577:g.12632C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.958C>G MANE Select	ENSP00000356671.3:p.Pro320Ala
ENST00000367698.3:c.958C>G	ENSP00000356671.3:p.Pro320Ala
ENST00000487183.1:n.609C>G
ENST00000617423.4:c.559+2117C>G	ENSP00000478688.1:n.559+2117C>G
NM_000488.3:c.958C>G , LRG_577t1:c.958C>G	NP_000479.1:p.Pro320Ala
XM_005245198.2:c.814C>G	XP_005245255.1:p.Pro272Ala
NM_001365052.1:c.814C>G	NP_001351981.1:p.Pro272Ala
NM_000488.4:c.958C>G MANE Select	NP_000479.1:p.Pro320Ala
NM_001365052.2:c.814C>G	NP_001351981.1:p.Pro272Ala
NM_001386302.1:c.1081C>G	NP_001373231.1:p.Pro361Ala
NM_001386303.1:c.1039C>G	NP_001373232.1:p.Pro347Ala
NM_001386304.1:c.937C>G	NP_001373233.1:p.Pro313Ala
NM_001386305.1:c.901C>G	NP_001373234.1:p.Pro301Ala
NM_001386306.1:c.742C>G	NP_001373235.1:p.Pro248Ala