Canonical Allele Identifier: CA14058793

Gene: SLC24A4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92486494C>A , CM000676.2:g.92486494C>A	GRCh38
NC_000014.8:g.92952838C>A , CM000676.1:g.92952838C>A	GRCh37
NC_000014.7:g.92022591C>A	NCBI36
NG_023408.1:g.168914C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532405.6:c.1423-172C>A MANE Select	ENSP00000431840.1:n.1423-172C>A
ENST00000676001.1:c.1423-172C>A	ENSP00000502715.1:n.1423-172C>A
ENST00000393265.6:c.1231-172C>A	ENSP00000376948.2:n.1231-172C>A
ENST00000525557.5:c.1019-172C>A
ENST00000526482.1:n.1677-172C>A
ENST00000531433.5:c.1366-172C>A	ENSP00000433302.1:n.1366-172C>A
ENST00000532405.5:c.1423-172C>A	ENSP00000431840.1:n.1423-172C>A
ENST00000554925.5:n.876-172C>A
NM_153646.3:c.1423-172C>A	NP_705932.2:n.1423-172C>A
NM_153647.3:c.1366-172C>A	NP_705933.2:n.1366-172C>A
NM_153648.3:c.1231-172C>A	NP_705934.1:n.1231-172C>A
XM_011536436.1:c.1564-172C>A	XP_011534738.1:n.1564-172C>A
XM_011536437.1:c.1507-172C>A	XP_011534739.1:n.1507-172C>A
XM_011536438.1:c.1564-172C>A	XP_011534740.1:n.1564-172C>A
XM_011536439.1:c.1507-172C>A	XP_011534741.1:n.1507-172C>A
XM_011536440.1:c.673-172C>A	XP_011534742.1:n.673-172C>A
XM_011536441.1:c.505-172C>A	XP_011534743.1:n.505-172C>A
XM_011536442.1:c.505-172C>A	XP_011534744.1:n.505-172C>A
XM_011536436.2:c.1564-172C>A	XP_011534738.1:n.1564-172C>A
XM_011536437.2:c.1507-172C>A	XP_011534739.1:n.1507-172C>A
XM_011536438.2:c.1564-172C>A	XP_011534740.1:n.1564-172C>A
XM_011536439.2:c.1507-172C>A	XP_011534741.1:n.1507-172C>A
XM_011536440.2:c.673-172C>A	XP_011534742.1:n.673-172C>A
XM_024449478.1:c.1366-172C>A	XP_024305246.1:n.1366-172C>A
NM_153647.4:c.1366-172C>A	NP_705933.2:n.1366-172C>A
NM_001378620.1:c.1423-172C>A	NP_001365549.1:n.1423-172C>A
NM_153646.4:c.1423-172C>A MANE Select	NP_705932.2:n.1423-172C>A
NM_153648.4:c.1231-172C>A	NP_705934.1:n.1231-172C>A