Canonical Allele Identifier: CA164209513

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1016150580
• MyVariant Identifiers: chr7:g.107304277_107304284del (hg19) ; chr7:g.107663832_107663839del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663836_107663843del , CM000669.2:g.107663836_107663843del	GRCh38
NC_000007.13:g.107304281_107304288del , CM000669.1:g.107304281_107304288del	GRCh37
NC_000007.12:g.107091517_107091524del	NCBI36
NG_008489.1:g.8202_8209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.304+401_304+408del MANE Select	ENSP00000494017.1:n.304+401_304+408del
ENST00000265715.7:c.304+401_304+408del	ENSP00000265715.3:n.304+401_304+408del
ENST00000440056.1:c.304+401_304+408del	ENSP00000394760.1:n.304+401_304+408del
NM_000441.1:c.304+401_304+408del	NP_000432.1:n.304+401_304+408del
XM_005250425.1:c.304+401_304+408del	XP_005250482.1:n.304+401_304+408del
XM_006716025.2:c.304+401_304+408del	XP_006716088.1:n.304+401_304+408del
XM_005250425.2:c.304+401_304+408del	XP_005250482.1:n.304+401_304+408del
XM_006716025.3:c.304+401_304+408del	XP_006716088.1:n.304+401_304+408del
XM_017012318.1:c.304+401_304+408del	XP_016867807.1:n.304+401_304+408del
NM_000441.2:c.304+401_304+408del MANE Select	NP_000432.1:n.304+401_304+408del