Canonical Allele Identifier: CA1732748123

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1791523293
• gnomAD v4: 7-107690032-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690034_107690036dup , CM000669.2:g.107690034_107690036dup	GRCh38
NC_000007.13:g.107330479_107330481dup , CM000669.1:g.107330479_107330481dup	GRCh37
NC_000007.12:g.107117715_107117717dup	NCBI36
NG_008489.1:g.34400_34402dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1150-90_1150-88dup MANE Select	ENSP00000494017.1:n.1150-90_1150-88dup
ENST00000265715.7:c.1150-90_1150-88dup	ENSP00000265715.3:n.1150-90_1150-88dup
NM_000441.1:c.1150-90_1150-88dup	NP_000432.1:n.1150-90_1150-88dup
XM_005250425.1:c.1150-90_1150-88dup	XP_005250482.1:n.1150-90_1150-88dup
XM_006716025.2:c.1150-90_1150-88dup	XP_006716088.1:n.1150-90_1150-88dup
XM_005250425.2:c.1150-90_1150-88dup	XP_005250482.1:n.1150-90_1150-88dup
XM_006716025.3:c.1150-90_1150-88dup	XP_006716088.1:n.1150-90_1150-88dup
XM_017012318.1:c.1150-90_1150-88dup	XP_016867807.1:n.1150-90_1150-88dup
NM_000441.2:c.1150-90_1150-88dup MANE Select	NP_000432.1:n.1150-90_1150-88dup