Canonical Allele Identifier: CA343773464

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878693G>T (hg19) ; chr1:g.173909555G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909555G>T , CM000663.2:g.173909555G>T	GRCh38
NC_000001.10:g.173878693G>T , CM000663.1:g.173878693G>T	GRCh37
NC_000001.9:g.172145316G>T	NCBI36
NG_012462.1:g.12824C>A , LRG_577:g.12824C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1150C>A MANE Select	ENSP00000356671.3:p.Pro384Thr
ENST00000367698.3:c.1150C>A	ENSP00000356671.3:p.Pro384Thr
ENST00000617423.4:c.560-2062C>A	ENSP00000478688.1:n.560-2062C>A
NM_000488.3:c.1150C>A , LRG_577t1:c.1150C>A	NP_000479.1:p.Pro384Thr
XM_005245198.2:c.1006C>A	XP_005245255.1:p.Pro336Thr
NM_001365052.1:c.1006C>A	NP_001351981.1:p.Pro336Thr
NM_000488.4:c.1150C>A MANE Select	NP_000479.1:p.Pro384Thr
NM_001365052.2:c.1006C>A	NP_001351981.1:p.Pro336Thr
NM_001386302.1:c.1273C>A	NP_001373231.1:p.Pro425Thr
NM_001386303.1:c.1231C>A	NP_001373232.1:p.Pro411Thr
NM_001386304.1:c.1129C>A	NP_001373233.1:p.Pro377Thr
NM_001386305.1:c.1093C>A	NP_001373234.1:p.Pro365Thr
NM_001386306.1:c.934C>A	NP_001373235.1:p.Pro312Thr