Canonical Allele Identifier: CA343773564

Gene: SERPINC1

Linked Data

• COSMIC: COSM5477802
• MyVariant Identifiers: chr1:g.173878738C>A (hg19) ; chr1:g.173909600C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909600C>A , CM000663.2:g.173909600C>A	GRCh38
NC_000001.10:g.173878738C>A , CM000663.1:g.173878738C>A	GRCh37
NC_000001.9:g.172145361C>A	NCBI36
NG_012462.1:g.12779G>T , LRG_577:g.12779G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1105G>T MANE Select	ENSP00000356671.3:p.Asp369Tyr
ENST00000367698.3:c.1105G>T	ENSP00000356671.3:p.Asp369Tyr
ENST00000617423.4:c.560-2107G>T	ENSP00000478688.1:n.560-2107G>T
NM_000488.3:c.1105G>T , LRG_577t1:c.1105G>T	NP_000479.1:p.Asp369Tyr
XM_005245198.2:c.961G>T	XP_005245255.1:p.Asp321Tyr
NM_001365052.1:c.961G>T	NP_001351981.1:p.Asp321Tyr
NM_000488.4:c.1105G>T MANE Select	NP_000479.1:p.Asp369Tyr
NM_001365052.2:c.961G>T	NP_001351981.1:p.Asp321Tyr
NM_001386302.1:c.1228G>T	NP_001373231.1:p.Asp410Tyr
NM_001386303.1:c.1186G>T	NP_001373232.1:p.Asp396Tyr
NM_001386304.1:c.1084G>T	NP_001373233.1:p.Asp362Tyr
NM_001386305.1:c.1048G>T	NP_001373234.1:p.Asp350Tyr
NM_001386306.1:c.889G>T	NP_001373235.1:p.Asp297Tyr