Canonical Allele Identifier: CA2777355211

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690351_107690352insG , CM000669.2:g.107690351_107690352insG	GRCh38
NC_000007.13:g.107330796_107330797insG , CM000669.1:g.107330796_107330797insG	GRCh37
NC_000007.12:g.107118032_107118033insG	NCBI36
NG_008489.1:g.34717_34718insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1263+114_1263+115insG MANE Select	ENSP00000494017.1:n.1263+114_1263+115insG
ENST00000265715.7:c.1263+114_1263+115insG	ENSP00000265715.3:n.1263+114_1263+115insG
NM_000441.1:c.1263+114_1263+115insG	NP_000432.1:n.1263+114_1263+115insG
XM_005250425.1:c.1263+114_1263+115insG	XP_005250482.1:n.1263+114_1263+115insG
XM_006716025.2:c.1263+114_1263+115insG	XP_006716088.1:n.1263+114_1263+115insG
XM_005250425.2:c.1263+114_1263+115insG	XP_005250482.1:n.1263+114_1263+115insG
XM_006716025.3:c.1263+114_1263+115insG	XP_006716088.1:n.1263+114_1263+115insG
XM_017012318.1:c.1263+114_1263+115insG	XP_016867807.1:n.1263+114_1263+115insG
NM_000441.2:c.1263+114_1263+115insG MANE Select	NP_000432.1:n.1263+114_1263+115insG