Canonical Allele Identifier: CA1315653809

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575319C= , CM000664.2:g.189575319C=	GRCh38
NC_000002.11:g.190440045C= , CM000664.1:g.190440045C=	GRCh37
NC_000002.10:g.190148290C=	NCBI36
NG_009027.1:g.10493G= , LRG_837:g.10493G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.113G= MANE Select	ENSP00000261024.3:p.Gly38=
ENST00000261024.6:c.113G=	ENSP00000261024.2:p.Gly38=
ENST00000418714.1:n.554G=
ENST00000427241.5:c.113G=	ENSP00000390005.1:p.Gly38=
ENST00000455320.5:c.113G=	ENSP00000413549.1:p.Gly38=
ENST00000479598.5:n.394G=
NM_014585.5:c.113G= , LRG_837t1:c.113G=	NP_055400.1:p.Gly38=
XM_005246505.1:c.-8G=	XP_005246562.1:n.-8G=
XM_005246505.2:c.-8G=	XP_005246562.1:n.-8G=
XM_017003938.2:c.-8G=	XP_016859427.1:n.-8G=
NM_014585.6:c.113G= MANE Select	NP_055400.1:p.Gly38=