Canonical Allele Identifier: CA1315653832

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575351A= , CM000664.2:g.189575351A=	GRCh38
NC_000002.11:g.190440077A= , CM000664.1:g.190440077A=	GRCh37
NC_000002.10:g.190148322A=	NCBI36
NG_009027.1:g.10461T= , LRG_837:g.10461T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.112-31T= MANE Select	ENSP00000261024.3:n.112-31T=
ENST00000261024.6:c.112-31T=	ENSP00000261024.2:n.112-31T=
ENST00000418714.1:n.553-31T=
ENST00000427241.5:c.112-31T=	ENSP00000390005.1:n.112-31T=
ENST00000455320.5:c.112-31T=	ENSP00000413549.1:n.112-31T=
ENST00000479598.5:n.393-31T=
NM_014585.5:c.112-31T= , LRG_837t1:c.112-31T=	NP_055400.1:n.112-31T=
XM_005246505.1:c.-9-31T=	XP_005246562.1:n.-9-31T=
XM_005246505.2:c.-9-31T=	XP_005246562.1:n.-9-31T=
XM_017003938.2:c.-9-31T=	XP_016859427.1:n.-9-31T=
NM_014585.6:c.112-31T= MANE Select	NP_055400.1:n.112-31T=