Canonical Allele Identifier: CA343772664

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873187C>G (hg19) ; chr1:g.173904049C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904049C>G , CM000663.2:g.173904049C>G	GRCh38
NC_000001.10:g.173873187C>G , CM000663.1:g.173873187C>G	GRCh37
NC_000001.9:g.172139810C>G	NCBI36
NG_012462.1:g.18330G>C , LRG_577:g.18330G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1235G>C MANE Select	ENSP00000356671.3:p.Ser412Thr
ENST00000367698.3:c.1235G>C	ENSP00000356671.3:p.Ser412Thr
ENST00000617423.4:c.620G>C	ENSP00000478688.1:p.Ser207Thr
NM_000488.3:c.1235G>C , LRG_577t1:c.1235G>C	NP_000479.1:p.Ser412Thr
XM_005245198.2:c.1091G>C	XP_005245255.1:p.Ser364Thr
NM_001365052.1:c.1091G>C	NP_001351981.1:p.Ser364Thr
NM_000488.4:c.1235G>C MANE Select	NP_000479.1:p.Ser412Thr
NM_001365052.2:c.1091G>C	NP_001351981.1:p.Ser364Thr
NM_001386302.1:c.1358G>C	NP_001373231.1:p.Ser453Thr
NM_001386303.1:c.1316G>C	NP_001373232.1:p.Ser439Thr
NM_001386304.1:c.1214G>C	NP_001373233.1:p.Ser405Thr
NM_001386305.1:c.1178G>C	NP_001373234.1:p.Ser393Thr
NM_001386306.1:c.1019G>C	NP_001373235.1:p.Ser340Thr