Canonical Allele Identifier: CA2715291771

Gene: SLC26A4

Linked Data

• dbSNP Id: rs200590284

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709871dup , CM000669.2:g.107709871dup	GRCh38
NC_000007.13:g.107350316dup , CM000669.1:g.107350316dup	GRCh37
NC_000007.12:g.107137552dup	NCBI36
NG_008489.1:g.54237dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-183dup MANE Select	ENSP00000494017.1:n.2090-183dup
ENST00000644846.1:c.746-183dup
ENST00000265715.7:c.2090-183dup	ENSP00000265715.3:n.2090-183dup
ENST00000492030.2:n.377-284dup
NM_000441.1:c.2090-183dup	NP_000432.1:n.2090-183dup
XM_005250425.1:c.2090-183dup	XP_005250482.1:n.2090-183dup
XM_005250425.2:c.2090-183dup	XP_005250482.1:n.2090-183dup
XM_017012318.1:c.2012-183dup	XP_016867807.1:n.2012-183dup
NM_000441.2:c.2090-183dup MANE Select	NP_000432.1:n.2090-183dup