Canonical Allele Identifier: CA421821614

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873186A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904048A>G , CM000663.2:g.173904048A>G	GRCh38
NC_000001.10:g.173873186A>G , CM000663.1:g.173873186A>G	GRCh37
NC_000001.9:g.172139809A>G	NCBI36
NG_012462.1:g.18331T>C , LRG_577:g.18331T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1236T>C MANE Select	ENSP00000356671.3:p.Ser412=
ENST00000367698.3:c.1236T>C	ENSP00000356671.3:p.Ser412=
ENST00000617423.4:c.621T>C	ENSP00000478688.1:p.Ser207=
NM_000488.3:c.1236T>C , LRG_577t1:c.1236T>C	NP_000479.1:p.Ser412=
XM_005245198.2:c.1092T>C	XP_005245255.1:p.Ser364=
NM_001365052.1:c.1092T>C	NP_001351981.1:p.Ser364=
NM_000488.4:c.1236T>C MANE Select	NP_000479.1:p.Ser412=
NM_001365052.2:c.1092T>C	NP_001351981.1:p.Ser364=
NM_001386302.1:c.1359T>C	NP_001373231.1:p.Ser453=
NM_001386303.1:c.1317T>C	NP_001373232.1:p.Ser439=
NM_001386304.1:c.1215T>C	NP_001373233.1:p.Ser405=
NM_001386305.1:c.1179T>C	NP_001373234.1:p.Ser393=
NM_001386306.1:c.1020T>C	NP_001373235.1:p.Ser340=