Canonical Allele Identifier: CA831167370

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1258073374
• MyVariant Identifiers: chr7:g.107302512_107302513del (hg19) ; chr7:g.107662067_107662068del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107662072_107662073del , CM000669.2:g.107662072_107662073del	GRCh38
NC_000007.13:g.107302517_107302518del , CM000669.1:g.107302517_107302518del	GRCh37
NC_000007.12:g.107089753_107089754del	NCBI36
NG_008489.1:g.6438_6439del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+267_164+268del MANE Select	ENSP00000494017.1:n.164+267_164+268del
ENST00000265715.7:c.164+267_164+268del	ENSP00000265715.3:n.164+267_164+268del
ENST00000440056.1:c.164+267_164+268del	ENSP00000394760.1:n.164+267_164+268del
NM_000441.1:c.164+267_164+268del	NP_000432.1:n.164+267_164+268del
XM_005250425.1:c.164+267_164+268del	XP_005250482.1:n.164+267_164+268del
XM_006716025.2:c.164+267_164+268del	XP_006716088.1:n.164+267_164+268del
XM_005250425.2:c.164+267_164+268del	XP_005250482.1:n.164+267_164+268del
XM_006716025.3:c.164+267_164+268del	XP_006716088.1:n.164+267_164+268del
XM_017012318.1:c.164+267_164+268del	XP_016867807.1:n.164+267_164+268del
NM_000441.2:c.164+267_164+268del MANE Select	NP_000432.1:n.164+267_164+268del