Canonical Allele Identifier: CA343773451

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878688A>G (hg19) ; chr1:g.173909550A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909550A>G , CM000663.2:g.173909550A>G	GRCh38
NC_000001.10:g.173878688A>G , CM000663.1:g.173878688A>G	GRCh37
NC_000001.9:g.172145311A>G	NCBI36
NG_012462.1:g.12829T>C , LRG_577:g.12829T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1153+2T>C MANE Select	ENSP00000356671.3:n.1153+2T>C
ENST00000367698.3:c.1153+2T>C	ENSP00000356671.3:n.1153+2T>C
ENST00000617423.4:c.560-2057T>C	ENSP00000478688.1:n.560-2057T>C
NM_000488.3:c.1153+2T>C , LRG_577t1:c.1153+2T>C	NP_000479.1:n.1153+2T>C
XM_005245198.2:c.1009+2T>C	XP_005245255.1:n.1009+2T>C
NM_001365052.1:c.1009+2T>C	NP_001351981.1:n.1009+2T>C
NM_000488.4:c.1153+2T>C MANE Select	NP_000479.1:n.1153+2T>C
NM_001365052.2:c.1009+2T>C	NP_001351981.1:n.1009+2T>C
NM_001386302.1:c.1276+2T>C	NP_001373231.1:n.1276+2T>C
NM_001386303.1:c.1234+2T>C	NP_001373232.1:n.1234+2T>C
NM_001386304.1:c.1132+2T>C	NP_001373233.1:n.1132+2T>C
NM_001386305.1:c.1096+2T>C	NP_001373234.1:n.1096+2T>C
NM_001386306.1:c.937+2T>C	NP_001373235.1:n.937+2T>C