Canonical Allele Identifier: CA163395

Gene: SLC24A4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92454034C>T , CM000676.2:g.92454034C>T	GRCh38
NC_000014.8:g.92920378C>T , CM000676.1:g.92920378C>T	GRCh37
NC_000014.7:g.91990131C>T	NCBI36
NG_023408.1:g.136454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532405.6:c.1015C>T MANE Select	ENSP00000431840.1:p.Arg339Ter
ENST00000676001.1:c.1015C>T	ENSP00000502715.1:p.Arg339Ter
ENST00000393265.6:c.823C>T	ENSP00000376948.2:p.Arg275Ter
ENST00000525557.5:c.611C>T
ENST00000526482.1:n.1269C>T
ENST00000531433.5:c.958C>T	ENSP00000433302.1:p.Arg320Ter
ENST00000532405.5:c.1015C>T	ENSP00000431840.1:p.Arg339Ter
ENST00000554925.5:n.468C>T
ENST00000556739.5:n.2564C>T
NM_153646.3:c.1015C>T	NP_705932.2:p.Arg339Ter
NM_153647.3:c.958C>T	NP_705933.2:p.Arg320Ter
NM_153648.3:c.823C>T	NP_705934.1:p.Arg275Ter
XM_005267342.1:c.571C>T	XP_005267399.1:p.Arg191Ter
XM_011536436.1:c.1156C>T	XP_011534738.1:p.Arg386Ter
XM_011536437.1:c.1099C>T	XP_011534739.1:p.Arg367Ter
XM_011536438.1:c.1156C>T	XP_011534740.1:p.Arg386Ter
XM_011536439.1:c.1099C>T	XP_011534741.1:p.Arg367Ter
XM_011536440.1:c.265C>T	XP_011534742.1:p.Arg89Ter
XM_011536441.1:c.97C>T	XP_011534743.1:p.Arg33Ter
XM_011536442.1:c.97C>T	XP_011534744.1:p.Arg33Ter
XM_005267342.2:c.571C>T	XP_005267399.1:p.Arg191Ter
XM_011536436.2:c.1156C>T	XP_011534738.1:p.Arg386Ter
XM_011536437.2:c.1099C>T	XP_011534739.1:p.Arg367Ter
XM_011536438.2:c.1156C>T	XP_011534740.1:p.Arg386Ter
XM_011536439.2:c.1099C>T	XP_011534741.1:p.Arg367Ter
XM_011536440.2:c.265C>T	XP_011534742.1:p.Arg89Ter
XM_024449478.1:c.958C>T	XP_024305246.1:p.Arg320Ter
NM_153647.4:c.958C>T	NP_705933.2:p.Arg320Ter
NM_001378620.1:c.1015C>T	NP_001365549.1:p.Arg339Ter
NM_153646.4:c.1015C>T MANE Select	NP_705932.2:p.Arg339Ter
NM_153648.4:c.823C>T	NP_705934.1:p.Arg275Ter