Canonical Allele Identifier: CA1315653632

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575175T= , CM000664.2:g.189575175T=	GRCh38
NC_000002.11:g.190439901T= , CM000664.1:g.190439901T=	GRCh37
NC_000002.10:g.190148146T=	NCBI36
NG_009027.1:g.10637A= , LRG_837:g.10637A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.257A= MANE Select	ENSP00000261024.3:p.Asn86=
ENST00000261024.6:c.257A=	ENSP00000261024.2:p.Asn86=
ENST00000418714.1:n.698A=
ENST00000427241.5:c.257A=	ENSP00000390005.1:p.Asn86=
ENST00000479598.5:n.538A=
NM_014585.5:c.257A= , LRG_837t1:c.257A=	NP_055400.1:p.Asn86=
XM_005246505.1:c.137A=	XP_005246562.1:p.Asn46=
XM_005246505.2:c.137A=	XP_005246562.1:p.Asn46=
XM_017003938.2:c.137A=	XP_016859427.1:p.Asn46=
NM_014585.6:c.257A= MANE Select	NP_055400.1:p.Asn86=