Canonical Allele Identifier: CA709966324
Gene: SLC24A4 HGNC NCBI

Linked Data

dbSNP Id: rs1261253332

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92467859A>T , CM000676.2:g.92467859A>T GRCh38
NC_000014.8:g.92934203A>T , CM000676.1:g.92934203A>T GRCh37
NC_000014.7:g.92003956A>T NCBI36
NG_023408.1:g.150279A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000532405.6:c.1255+11251A>T MANE Select ENSP00000431840.1:n.1255+11251A>T
ENST00000676001.1:c.1255+11251A>T ENSP00000502715.1:n.1255+11251A>T
ENST00000393265.6:c.1063+11251A>T ENSP00000376948.2:n.1063+11251A>T
ENST00000525557.5:c.851+11251A>T
ENST00000526482.1:n.1509+11251A>T
ENST00000531433.5:c.1198+11251A>T ENSP00000433302.1:n.1198+11251A>T
ENST00000532405.5:c.1255+11251A>T ENSP00000431840.1:n.1255+11251A>T
ENST00000554925.5:n.708+11251A>T
NM_153646.3:c.1255+11251A>T NP_705932.2:n.1255+11251A>T
NM_153647.3:c.1198+11251A>T NP_705933.2:n.1198+11251A>T
NM_153648.3:c.1063+11251A>T NP_705934.1:n.1063+11251A>T
XM_005267342.1:c.811+11251A>T XP_005267399.1:n.811+11251A>T
XM_011536436.1:c.1396+11251A>T XP_011534738.1:n.1396+11251A>T
XM_011536437.1:c.1339+11251A>T XP_011534739.1:n.1339+11251A>T
XM_011536438.1:c.1396+11251A>T XP_011534740.1:n.1396+11251A>T
XM_011536439.1:c.1339+11251A>T XP_011534741.1:n.1339+11251A>T
XM_011536440.1:c.505+11251A>T XP_011534742.1:n.505+11251A>T
XM_011536441.1:c.337+11251A>T XP_011534743.1:n.337+11251A>T
XM_011536442.1:c.337+11251A>T XP_011534744.1:n.337+11251A>T
XM_005267342.2:c.811+11251A>T XP_005267399.1:n.811+11251A>T
XM_011536436.2:c.1396+11251A>T XP_011534738.1:n.1396+11251A>T
XM_011536437.2:c.1339+11251A>T XP_011534739.1:n.1339+11251A>T
XM_011536438.2:c.1396+11251A>T XP_011534740.1:n.1396+11251A>T
XM_011536439.2:c.1339+11251A>T XP_011534741.1:n.1339+11251A>T
XM_011536440.2:c.505+11251A>T XP_011534742.1:n.505+11251A>T
XM_024449478.1:c.1198+11251A>T XP_024305246.1:n.1198+11251A>T
NM_153647.4:c.1198+11251A>T NP_705933.2:n.1198+11251A>T
NM_001378620.1:c.1255+11251A>T NP_001365549.1:n.1255+11251A>T
NM_153646.4:c.1255+11251A>T MANE Select NP_705932.2:n.1255+11251A>T
NM_153648.4:c.1063+11251A>T NP_705934.1:n.1063+11251A>T