Canonical Allele Identifier: CA2684468537

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107710005-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107710005_107710006insC , CM000669.2:g.107710005_107710006insC	GRCh38
NC_000007.13:g.107350450_107350451insC , CM000669.1:g.107350450_107350451insC	GRCh37
NC_000007.12:g.107137686_107137687insC	NCBI36
NG_008489.1:g.54371_54372insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-49_2090-48insC MANE Select	ENSP00000494017.1:n.2090-49_2090-48insC
ENST00000644846.1:c.746-49_746-48insC
ENST00000265715.7:c.2090-49_2090-48insC	ENSP00000265715.3:n.2090-49_2090-48insC
ENST00000492030.2:n.377-150_377-149insC
NM_000441.1:c.2090-49_2090-48insC	NP_000432.1:n.2090-49_2090-48insC
XM_005250425.1:c.2090-49_2090-48insC	XP_005250482.1:n.2090-49_2090-48insC
XM_005250425.2:c.2090-49_2090-48insC	XP_005250482.1:n.2090-49_2090-48insC
XM_017012318.1:c.2012-49_2012-48insC	XP_016867807.1:n.2012-49_2012-48insC
NM_000441.2:c.2090-49_2090-48insC MANE Select	NP_000432.1:n.2090-49_2090-48insC