Canonical Allele Identifier: CA1315653765

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575265T= , CM000664.2:g.189575265T=	GRCh38
NC_000002.11:g.190439991T= , CM000664.1:g.190439991T=	GRCh37
NC_000002.10:g.190148236T=	NCBI36
NG_009027.1:g.10547A= , LRG_837:g.10547A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.167A= MANE Select	ENSP00000261024.3:p.Asn56=
ENST00000261024.6:c.167A=	ENSP00000261024.2:p.Asn56=
ENST00000418714.1:n.608A=
ENST00000427241.5:c.167A=	ENSP00000390005.1:p.Asn56=
ENST00000479598.5:n.448A=
NM_014585.5:c.167A= , LRG_837t1:c.167A=	NP_055400.1:p.Asn56=
XM_005246505.1:c.47A=	XP_005246562.1:p.Asn16=
XM_005246505.2:c.47A=	XP_005246562.1:p.Asn16=
XM_017003938.2:c.47A=	XP_016859427.1:p.Asn16=
NM_014585.6:c.167A= MANE Select	NP_055400.1:p.Asn56=