Canonical Allele Identifier: CA2684466486

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107690043-TAATGTACTTCCTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690047_107690060del , CM000669.2:g.107690047_107690060del	GRCh38
NC_000007.13:g.107330492_107330505del , CM000669.1:g.107330492_107330505del	GRCh37
NC_000007.12:g.107117728_107117741del	NCBI36
NG_008489.1:g.34413_34426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1150-77_1150-64del MANE Select	ENSP00000494017.1:n.1150-77_1150-64del
ENST00000265715.7:c.1150-77_1150-64del	ENSP00000265715.3:n.1150-77_1150-64del
NM_000441.1:c.1150-77_1150-64del	NP_000432.1:n.1150-77_1150-64del
XM_005250425.1:c.1150-77_1150-64del	XP_005250482.1:n.1150-77_1150-64del
XM_006716025.2:c.1150-77_1150-64del	XP_006716088.1:n.1150-77_1150-64del
XM_005250425.2:c.1150-77_1150-64del	XP_005250482.1:n.1150-77_1150-64del
XM_006716025.3:c.1150-77_1150-64del	XP_006716088.1:n.1150-77_1150-64del
XM_017012318.1:c.1150-77_1150-64del	XP_016867807.1:n.1150-77_1150-64del
NM_000441.2:c.1150-77_1150-64del MANE Select	NP_000432.1:n.1150-77_1150-64del