Canonical Allele Identifier: CA421942722

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878937A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909799A>C , CM000663.2:g.173909799A>C	GRCh38
NC_000001.10:g.173878937A>C , CM000663.1:g.173878937A>C	GRCh37
NC_000001.9:g.172145560A>C	NCBI36
NG_012462.1:g.12580T>G , LRG_577:g.12580T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.906T>G MANE Select	ENSP00000356671.3:p.Leu302=
ENST00000367698.3:c.906T>G	ENSP00000356671.3:p.Leu302=
ENST00000487183.1:n.557T>G
ENST00000617423.4:c.559+2065T>G	ENSP00000478688.1:n.559+2065T>G
NM_000488.3:c.906T>G , LRG_577t1:c.906T>G	NP_000479.1:p.Leu302=
XM_005245198.2:c.762T>G	XP_005245255.1:p.Leu254=
NM_001365052.1:c.762T>G	NP_001351981.1:p.Leu254=
NM_000488.4:c.906T>G MANE Select	NP_000479.1:p.Leu302=
NM_001365052.2:c.762T>G	NP_001351981.1:p.Leu254=
NM_001386302.1:c.1029T>G	NP_001373231.1:p.Leu343=
NM_001386303.1:c.987T>G	NP_001373232.1:p.Leu329=
NM_001386304.1:c.885T>G	NP_001373233.1:p.Leu295=
NM_001386305.1:c.849T>G	NP_001373234.1:p.Leu283=
NM_001386306.1:c.690T>G	NP_001373235.1:p.Leu230=