Canonical Allele Identifier: CA343774281

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657687871
• MyVariant Identifiers: chr1:g.173878930G>T (hg19) ; chr1:g.173909792G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909792G>T , CM000663.2:g.173909792G>T	GRCh38
NC_000001.10:g.173878930G>T , CM000663.1:g.173878930G>T	GRCh37
NC_000001.9:g.172145553G>T	NCBI36
NG_012462.1:g.12587C>A , LRG_577:g.12587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.913C>A MANE Select	ENSP00000356671.3:p.Pro305Thr
ENST00000367698.3:c.913C>A	ENSP00000356671.3:p.Pro305Thr
ENST00000487183.1:n.564C>A
ENST00000617423.4:c.559+2072C>A	ENSP00000478688.1:n.559+2072C>A
NM_000488.3:c.913C>A , LRG_577t1:c.913C>A	NP_000479.1:p.Pro305Thr
XM_005245198.2:c.769C>A	XP_005245255.1:p.Pro257Thr
NM_001365052.1:c.769C>A	NP_001351981.1:p.Pro257Thr
NM_000488.4:c.913C>A MANE Select	NP_000479.1:p.Pro305Thr
NM_001365052.2:c.769C>A	NP_001351981.1:p.Pro257Thr
NM_001386302.1:c.1036C>A	NP_001373231.1:p.Pro346Thr
NM_001386303.1:c.994C>A	NP_001373232.1:p.Pro332Thr
NM_001386304.1:c.892C>A	NP_001373233.1:p.Pro298Thr
NM_001386305.1:c.856C>A	NP_001373234.1:p.Pro286Thr
NM_001386306.1:c.697C>A	NP_001373235.1:p.Pro233Thr