Canonical Allele Identifier: CA3206786715

Gene: SLC24A4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92486738A= , CM000676.2:g.92486738A=	GRCh38
NC_000014.8:g.92953082A= , CM000676.1:g.92953082A=	GRCh37
NC_000014.7:g.92022835A=	NCBI36
NG_023408.1:g.169158A=

Transcript Alleles

HGVS	Amino-acid Change
NM_153646.4:c.1495A= MANE Select	NP_705932.2:p.Ser499=
ENST00000532405.6:c.1495A= MANE Select	ENSP00000431840.1:p.Ser499=
NM_001378620.1:c.1495A=	NP_001365549.1:p.Ser499=
NM_153646.3:c.1495A=	NP_705932.2:p.Ser499=
NM_153647.3:c.1438A=	NP_705933.2:p.Ser480=
NM_153647.4:c.1438A=	NP_705933.2:p.Ser480=
NM_153648.3:c.1303A=	NP_705934.1:p.Ser435=
NM_153648.4:c.1303A=	NP_705934.1:p.Ser435=
ENST00000393265.6:c.1303A=	ENSP00000376948.2:p.Ser435=
ENST00000525557.5:c.1091A=
ENST00000526482.1:n.1749A=
ENST00000531433.5:c.1438A=	ENSP00000433302.1:p.Ser480=
ENST00000532405.5:c.1495A=	ENSP00000431840.1:p.Ser499=
ENST00000554925.5:n.948A=
ENST00000676001.1:c.1495A=	ENSP00000502715.1:p.Ser499=
XM_011536436.1:c.1636A=	XP_011534738.1:p.Ser546=
XM_011536436.2:c.1636A=	XP_011534738.1:p.Ser546=
XM_011536437.1:c.1579A=	XP_011534739.1:p.Ser527=
XM_011536437.2:c.1579A=	XP_011534739.1:p.Ser527=
XM_011536438.1:c.1636A=	XP_011534740.1:p.Ser546=
XM_011536438.2:c.1636A=	XP_011534740.1:p.Ser546=
XM_011536439.1:c.1579A=	XP_011534741.1:p.Ser527=
XM_011536439.2:c.1579A=	XP_011534741.1:p.Ser527=
XM_011536440.1:c.745A=	XP_011534742.1:p.Ser249=
XM_011536440.2:c.745A=	XP_011534742.1:p.Ser249=
XM_011536441.1:c.577A=	XP_011534743.1:p.Ser193=
XM_011536442.1:c.577A=	XP_011534744.1:p.Ser193=
XM_024449478.1:c.1438A=	XP_024305246.1:p.Ser480=