Canonical Allele Identifier: CA1732750879

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709777_107709778delinsGA , CM000669.2:g.107709777_107709778delinsGA	GRCh38
NC_000007.13:g.107350222_107350223delinsGA , CM000669.1:g.107350222_107350223delinsGA	GRCh37
NC_000007.12:g.107137458_107137459delinsGA	NCBI36
NG_008489.1:g.54143_54144delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-277_2090-276delinsGA MANE Select	ENSP00000494017.1:n.2090-277_2090-276delinsGA
ENST00000644846.1:c.746-277_746-276delinsGA
ENST00000265715.7:c.2090-277_2090-276delinsGA	ENSP00000265715.3:n.2090-277_2090-276delinsGA
ENST00000492030.2:n.377-378_377-377delinsGA
NM_000441.1:c.2090-277_2090-276delinsGA	NP_000432.1:n.2090-277_2090-276delinsGA
XM_005250425.1:c.2090-277_2090-276delinsGA	XP_005250482.1:n.2090-277_2090-276delinsGA
XM_005250425.2:c.2090-277_2090-276delinsGA	XP_005250482.1:n.2090-277_2090-276delinsGA
XM_017012318.1:c.2012-277_2012-276delinsGA	XP_016867807.1:n.2012-277_2012-276delinsGA
NM_000441.2:c.2090-277_2090-276delinsGA MANE Select	NP_000432.1:n.2090-277_2090-276delinsGA