Canonical Allele Identifier: CA343776225

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173880969A>C (hg19) ; chr1:g.173911831A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911831A>C , CM000663.2:g.173911831A>C	GRCh38
NC_000001.10:g.173880969A>C , CM000663.1:g.173880969A>C	GRCh37
NC_000001.9:g.172147592A>C	NCBI36
NG_012462.1:g.10548T>G , LRG_577:g.10548T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.592T>G MANE Select	ENSP00000356671.3:p.Tyr198Asp
ENST00000367698.3:c.592T>G	ENSP00000356671.3:p.Tyr198Asp
ENST00000487183.1:n.297T>G
ENST00000617423.4:c.559+33T>G	ENSP00000478688.1:n.559+33T>G
NM_000488.3:c.592T>G , LRG_577t1:c.592T>G	NP_000479.1:p.Tyr198Asp
XM_005245198.2:c.448T>G	XP_005245255.1:p.Tyr150Asp
NM_001365052.1:c.448T>G	NP_001351981.1:p.Tyr150Asp
NM_000488.4:c.592T>G MANE Select	NP_000479.1:p.Tyr198Asp
NM_001365052.2:c.448T>G	NP_001351981.1:p.Tyr150Asp
NM_001386302.1:c.592T>G	NP_001373231.1:p.Tyr198Asp
NM_001386303.1:c.673T>G	NP_001373232.1:p.Tyr225Asp
NM_001386304.1:c.592T>G	NP_001373233.1:p.Tyr198Asp
NM_001386305.1:c.592T>G	NP_001373234.1:p.Tyr198Asp
NM_001386306.1:c.409-940T>G	NP_001373235.1:n.409-940T>G