Canonical Allele Identifier: CA392449696

Gene: SLC24A5

Linked Data

• MyVariant Identifiers: chr15:g.48426485C>T (hg19) ; chr15:g.48134288C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48134288C>T , CM000677.2:g.48134288C>T	GRCh38
NC_000015.9:g.48426485C>T , CM000677.1:g.48426485C>T	GRCh37
NC_000015.8:g.46213777C>T	NCBI36
NG_011500.1:g.18317C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000341459.8:c.332C>T MANE Select	ENSP00000341550.3:p.Thr111Ile
ENST00000341459.7:c.332C>T	ENSP00000341550.3:p.Thr111Ile
ENST00000449382.2:c.152C>T	ENSP00000389966.2:p.Thr51Ile
ENST00000463289.1:n.92C>T
NM_205850.2:c.332C>T	NP_995322.1:p.Thr111Ile
XM_011521458.1:c.332C>T	XP_011519760.1:p.Thr111Ile
XM_017022079.1:c.-8C>T	XP_016877568.1:n.-8C>T
XM_017022080.1:c.-8C>T	XP_016877569.1:n.-8C>T
XM_024449901.1:c.-8C>T	XP_024305669.1:n.-8C>T
NM_205850.3:c.332C>T MANE Select	NP_995322.1:p.Thr111Ile