Canonical Allele Identifier: CA343774517

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878988G>C (hg19) ; chr1:g.173909850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909850G>C , CM000663.2:g.173909850G>C	GRCh38
NC_000001.10:g.173878988G>C , CM000663.1:g.173878988G>C	GRCh37
NC_000001.9:g.172145611G>C	NCBI36
NG_012462.1:g.12529C>G , LRG_577:g.12529C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.855C>G MANE Select	ENSP00000356671.3:p.Tyr285Ter
ENST00000367698.3:c.855C>G	ENSP00000356671.3:p.Tyr285Ter
ENST00000487183.1:n.506C>G
ENST00000617423.4:c.559+2014C>G	ENSP00000478688.1:n.559+2014C>G
NM_000488.3:c.855C>G , LRG_577t1:c.855C>G	NP_000479.1:p.Tyr285Ter
XM_005245198.2:c.711C>G	XP_005245255.1:p.Tyr237Ter
NM_001365052.1:c.711C>G	NP_001351981.1:p.Tyr237Ter
NM_000488.4:c.855C>G MANE Select	NP_000479.1:p.Tyr285Ter
NM_001365052.2:c.711C>G	NP_001351981.1:p.Tyr237Ter
NM_001386302.1:c.978C>G	NP_001373231.1:p.Tyr326Ter
NM_001386303.1:c.936C>G	NP_001373232.1:p.Tyr312Ter
NM_001386304.1:c.834C>G	NP_001373233.1:p.Tyr278Ter
NM_001386305.1:c.798C>G	NP_001373234.1:p.Tyr266Ter
NM_001386306.1:c.639C>G	NP_001373235.1:p.Tyr213Ter