Canonical Allele Identifier: CA1315653822

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189563623C= , CM000664.2:g.189563623C=	GRCh38
NC_000002.11:g.190428349C= , CM000664.1:g.190428349C=	GRCh37
NC_000002.10:g.190136594C=	NCBI36
NG_009027.1:g.22189G= , LRG_837:g.22189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.1363G= MANE Select	ENSP00000261024.3:p.Val455=
ENST00000261024.6:c.1363G=	ENSP00000261024.2:p.Val455=
NM_014585.5:c.1363G= , LRG_837t1:c.1363G=	NP_055400.1:p.Val455=
XM_005246505.1:c.1243G=	XP_005246562.1:p.Val415=
XM_005246505.2:c.1243G=	XP_005246562.1:p.Val415=
XM_017003938.2:c.1243G=	XP_016859427.1:p.Val415=
NM_014585.6:c.1363G= MANE Select	NP_055400.1:p.Val455=