Canonical Allele Identifier: CA2684468483

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107709923-G-GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709923_107709924insCA , CM000669.2:g.107709923_107709924insCA	GRCh38
NC_000007.13:g.107350368_107350369insCA , CM000669.1:g.107350368_107350369insCA	GRCh37
NC_000007.12:g.107137604_107137605insCA	NCBI36
NG_008489.1:g.54289_54290insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-131_2090-130insCA MANE Select	ENSP00000494017.1:n.2090-131_2090-130insCA
ENST00000644846.1:c.746-131_746-130insCA
ENST00000265715.7:c.2090-131_2090-130insCA	ENSP00000265715.3:n.2090-131_2090-130insCA
ENST00000492030.2:n.377-232_377-231insCA
NM_000441.1:c.2090-131_2090-130insCA	NP_000432.1:n.2090-131_2090-130insCA
XM_005250425.1:c.2090-131_2090-130insCA	XP_005250482.1:n.2090-131_2090-130insCA
XM_005250425.2:c.2090-131_2090-130insCA	XP_005250482.1:n.2090-131_2090-130insCA
XM_017012318.1:c.2012-131_2012-130insCA	XP_016867807.1:n.2012-131_2012-130insCA
NM_000441.2:c.2090-131_2090-130insCA MANE Select	NP_000432.1:n.2090-131_2090-130insCA