Canonical Allele Identifier: CA368832127

Gene: SLC26A4

Linked Data

• dbSNP Id: rs763276250
• MyVariant Identifiers: chr7:g.107315553A>T (hg19) ; chr7:g.107675108A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107675108A>T , CM000669.2:g.107675108A>T	GRCh38
NC_000007.13:g.107315553A>T , CM000669.1:g.107315553A>T	GRCh37
NC_000007.12:g.107102789A>T	NCBI36
NG_008489.1:g.19474A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.764A>T MANE Select	ENSP00000494017.1:p.Tyr255Phe
ENST00000265715.7:c.764A>T	ENSP00000265715.3:p.Tyr255Phe
NM_000441.1:c.764A>T	NP_000432.1:p.Tyr255Phe
XM_005250425.1:c.764A>T	XP_005250482.1:p.Tyr255Phe
XM_006716025.2:c.764A>T	XP_006716088.1:p.Tyr255Phe
XM_005250425.2:c.764A>T	XP_005250482.1:p.Tyr255Phe
XM_006716025.3:c.764A>T	XP_006716088.1:p.Tyr255Phe
XM_017012318.1:c.764A>T	XP_016867807.1:p.Tyr255Phe
NM_000441.2:c.764A>T MANE Select	NP_000432.1:p.Tyr255Phe