Canonical Allele Identifier: CA2581187965

Gene: SLC24A4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92377484G= , CM000676.2:g.92377484G=	GRCh38
NC_000014.8:g.92843828G= , CM000676.1:g.92843828G=	GRCh37
NC_000014.7:g.91913581G=	NCBI36
NG_023408.1:g.59904G=

Transcript Alleles

HGVS	Amino-acid Change
NM_153646.4:c.241+51506G= MANE Select	NP_705932.2:n.241+51506G=
ENST00000532405.6:c.241+51506G= MANE Select	ENSP00000431840.1:n.241+51506G=
NM_001378620.1:c.241+51506G=	NP_001365549.1:n.241+51506G=
NM_153646.3:c.241+51506G=	NP_705932.2:n.241+51506G=
NM_153647.3:c.241+51506G=	NP_705933.2:n.241+51506G=
NM_153647.4:c.241+51506G=	NP_705933.2:n.241+51506G=
NM_153648.3:c.49+51506G=	NP_705934.1:n.49+51506G=
NM_153648.4:c.49+51506G=	NP_705934.1:n.49+51506G=
ENST00000393265.6:c.49+51506G=	ENSP00000376948.2:n.49+51506G=
ENST00000531433.5:c.241+51506G=	ENSP00000433302.1:n.241+51506G=
ENST00000532405.5:c.241+51506G=	ENSP00000431840.1:n.241+51506G=
ENST00000676001.1:c.241+51506G=	ENSP00000502715.1:n.241+51506G=
XM_011536436.1:c.382+51506G=	XP_011534738.1:n.382+51506G=
XM_011536436.2:c.382+51506G=	XP_011534738.1:n.382+51506G=
XM_011536437.1:c.382+51506G=	XP_011534739.1:n.382+51506G=
XM_011536437.2:c.382+51506G=	XP_011534739.1:n.382+51506G=
XM_011536438.1:c.382+51506G=	XP_011534740.1:n.382+51506G=
XM_011536438.2:c.382+51506G=	XP_011534740.1:n.382+51506G=
XM_011536439.1:c.382+51506G=	XP_011534741.1:n.382+51506G=
XM_011536439.2:c.382+51506G=	XP_011534741.1:n.382+51506G=
XM_024449478.1:c.241+51506G=	XP_024305246.1:n.241+51506G=