Canonical Allele Identifier: CA3206786707

Gene: SLC24A4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92442132C= , CM000676.2:g.92442132C=	GRCh38
NC_000014.8:g.92908476C= , CM000676.1:g.92908476C=	GRCh37
NC_000014.7:g.91978229C=	NCBI36
NG_023408.1:g.124552C=

Transcript Alleles

HGVS	Amino-acid Change
NM_153646.4:c.437C= MANE Select	NP_705932.2:p.Ala146=
ENST00000532405.6:c.437C= MANE Select	ENSP00000431840.1:p.Ala146=
NM_001378620.1:c.437C=	NP_001365549.1:p.Ala146=
NM_153646.3:c.437C=	NP_705932.2:p.Ala146=
NM_153647.3:c.437C=	NP_705933.2:p.Ala146=
NM_153647.4:c.437C=	NP_705933.2:p.Ala146=
NM_153648.3:c.245C=	NP_705934.1:p.Ala82=
NM_153648.4:c.245C=	NP_705934.1:p.Ala82=
ENST00000393265.6:c.245C=	ENSP00000376948.2:p.Ala82=
ENST00000525557.5:c.90C=
ENST00000531433.5:c.437C=	ENSP00000433302.1:p.Ala146=
ENST00000532405.5:c.437C=	ENSP00000431840.1:p.Ala146=
ENST00000554461.5:c.110C=	ENSP00000452099.1:p.Ala37=
ENST00000676001.1:c.437C=	ENSP00000502715.1:p.Ala146=
XM_005267342.1:c.110C=	XP_005267399.1:p.Ala37=
XM_005267342.2:c.110C=	XP_005267399.1:p.Ala37=
XM_011536436.1:c.578C=	XP_011534738.1:p.Ala193=
XM_011536436.2:c.578C=	XP_011534738.1:p.Ala193=
XM_011536437.1:c.578C=	XP_011534739.1:p.Ala193=
XM_011536437.2:c.578C=	XP_011534739.1:p.Ala193=
XM_011536438.1:c.578C=	XP_011534740.1:p.Ala193=
XM_011536438.2:c.578C=	XP_011534740.1:p.Ala193=
XM_011536439.1:c.578C=	XP_011534741.1:p.Ala193=
XM_011536439.2:c.578C=	XP_011534741.1:p.Ala193=
XM_024449478.1:c.437C=	XP_024305246.1:p.Ala146=