Canonical Allele Identifier: CA2684468529

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107709986-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709988_107709989del , CM000669.2:g.107709988_107709989del	GRCh38
NC_000007.13:g.107350433_107350434del , CM000669.1:g.107350433_107350434del	GRCh37
NC_000007.12:g.107137669_107137670del	NCBI36
NG_008489.1:g.54354_54355del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-66_2090-65del MANE Select	ENSP00000494017.1:n.2090-66_2090-65del
ENST00000644846.1:c.746-66_746-65del
ENST00000265715.7:c.2090-66_2090-65del	ENSP00000265715.3:n.2090-66_2090-65del
ENST00000492030.2:n.377-167_377-166del
NM_000441.1:c.2090-66_2090-65del	NP_000432.1:n.2090-66_2090-65del
XM_005250425.1:c.2090-66_2090-65del	XP_005250482.1:n.2090-66_2090-65del
XM_005250425.2:c.2090-66_2090-65del	XP_005250482.1:n.2090-66_2090-65del
XM_017012318.1:c.2012-66_2012-65del	XP_016867807.1:n.2012-66_2012-65del
NM_000441.2:c.2090-66_2090-65del MANE Select	NP_000432.1:n.2090-66_2090-65del