Canonical Allele Identifier: CA1315653799

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575309C= , CM000664.2:g.189575309C=	GRCh38
NC_000002.11:g.190440035C= , CM000664.1:g.190440035C=	GRCh37
NC_000002.10:g.190148280C=	NCBI36
NG_009027.1:g.10503G= , LRG_837:g.10503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.123G= MANE Select	ENSP00000261024.3:p.Met41=
ENST00000261024.6:c.123G=	ENSP00000261024.2:p.Met41=
ENST00000418714.1:n.564G=
ENST00000427241.5:c.123G=	ENSP00000390005.1:p.Met41=
ENST00000455320.5:c.123G=	ENSP00000413549.1:p.Met41=
ENST00000479598.5:n.404G=
NM_014585.5:c.123G= , LRG_837t1:c.123G=	NP_055400.1:p.Met41=
XM_005246505.1:c.3G=	XP_005246562.1:p.Met1=
XM_005246505.2:c.3G=	XP_005246562.1:p.Met1=
XM_017003938.2:c.3G=	XP_016859427.1:p.Met1=
NM_014585.6:c.123G= MANE Select	NP_055400.1:p.Met41=