Canonical Allele Identifier: CA343772349

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873103A>G (hg19) ; chr1:g.173903965A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903965A>G , CM000663.2:g.173903965A>G	GRCh38
NC_000001.10:g.173873103A>G , CM000663.1:g.173873103A>G	GRCh37
NC_000001.9:g.172139726A>G	NCBI36
NG_012462.1:g.18414T>C , LRG_577:g.18414T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1319T>C MANE Select	ENSP00000356671.3:p.Phe440Ser
ENST00000367698.3:c.1319T>C	ENSP00000356671.3:p.Phe440Ser
ENST00000617423.4:c.704T>C	ENSP00000478688.1:p.Phe235Ser
NM_000488.3:c.1319T>C , LRG_577t1:c.1319T>C	NP_000479.1:p.Phe440Ser
XM_005245198.2:c.1175T>C	XP_005245255.1:p.Phe392Ser
NM_001365052.1:c.1175T>C	NP_001351981.1:p.Phe392Ser
NM_000488.4:c.1319T>C MANE Select	NP_000479.1:p.Phe440Ser
NM_001365052.2:c.1175T>C	NP_001351981.1:p.Phe392Ser
NM_001386302.1:c.1442T>C	NP_001373231.1:p.Phe481Ser
NM_001386303.1:c.1400T>C	NP_001373232.1:p.Phe467Ser
NM_001386304.1:c.1298T>C	NP_001373233.1:p.Phe433Ser
NM_001386305.1:c.1262T>C	NP_001373234.1:p.Phe421Ser
NM_001386306.1:c.1103T>C	NP_001373235.1:p.Phe368Ser