Canonical Allele Identifier: CA2684468481

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107709922-G-GTTCACT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709922_107709923insTTCACT , CM000669.2:g.107709922_107709923insTTCACT	GRCh38
NC_000007.13:g.107350367_107350368insTTCACT , CM000669.1:g.107350367_107350368insTTCACT	GRCh37
NC_000007.12:g.107137603_107137604insTTCACT	NCBI36
NG_008489.1:g.54288_54289insTTCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-132_2090-131insTTCACT MANE Select	ENSP00000494017.1:n.2090-132_2090-131insTTCACT
ENST00000644846.1:c.746-132_746-131insTTCACT
ENST00000265715.7:c.2090-132_2090-131insTTCACT	ENSP00000265715.3:n.2090-132_2090-131insTTCACT
ENST00000492030.2:n.377-233_377-232insTTCACT
NM_000441.1:c.2090-132_2090-131insTTCACT	NP_000432.1:n.2090-132_2090-131insTTCACT
XM_005250425.1:c.2090-132_2090-131insTTCACT	XP_005250482.1:n.2090-132_2090-131insTTCACT
XM_005250425.2:c.2090-132_2090-131insTTCACT	XP_005250482.1:n.2090-132_2090-131insTTCACT
XM_017012318.1:c.2012-132_2012-131insTTCACT	XP_016867807.1:n.2012-132_2012-131insTTCACT
NM_000441.2:c.2090-132_2090-131insTTCACT MANE Select	NP_000432.1:n.2090-132_2090-131insTTCACT