Canonical Allele Identifier: CA457104587

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107710097-C-T
• MyVariant Identifiers: chr7:g.107350542C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107710097C>T , CM000669.2:g.107710097C>T	GRCh38
NC_000007.13:g.107350542C>T , CM000669.1:g.107350542C>T	GRCh37
NC_000007.12:g.107137778C>T	NCBI36
NG_008489.1:g.54463C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2133C>T MANE Select	ENSP00000494017.1:p.Asp711=
ENST00000644846.1:c.789C>T
ENST00000265715.7:c.2133C>T	ENSP00000265715.3:p.Asp711=
ENST00000492030.2:n.377-58C>T
NM_000441.1:c.2133C>T	NP_000432.1:p.Asp711=
XM_005250425.1:c.2133C>T	XP_005250482.1:p.Asp711=
XM_005250425.2:c.2133C>T	XP_005250482.1:p.Asp711=
XM_017012318.1:c.2055C>T	XP_016867807.1:p.Asp685=
NM_000441.2:c.2133C>T MANE Select	NP_000432.1:p.Asp711=