Canonical Allele Identifier: CA1105620949

Gene: SLC26A4

Linked Data

• gnomAD v3: 7-107701755-G-GTCGCCGT
• gnomAD v4: 7-107701755-G-GTCGCCGT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701755_107701756insTCGCCGT , CM000669.2:g.107701755_107701756insTCGCCGT	GRCh38
NC_000007.13:g.107342200_107342201insTCGCCGT , CM000669.1:g.107342200_107342201insTCGCCGT	GRCh37
NC_000007.12:g.107129436_107129437insTCGCCGT	NCBI36
NG_008489.1:g.46121_46122insTCGCCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1804-72_1804-71insTCGCCGT MANE Select	ENSP00000494017.1:n.1804-72_1804-71insTCGCCGT
ENST00000644846.1:c.515-72_515-71insTCGCCGT
ENST00000265715.7:c.1804-72_1804-71insTCGCCGT	ENSP00000265715.3:n.1804-72_1804-71insTCGCCGT
ENST00000480841.5:n.653-72_653-71insTCGCCGT
ENST00000492030.2:n.91-72_91-71insTCGCCGT
NM_000441.1:c.1804-72_1804-71insTCGCCGT	NP_000432.1:n.1804-72_1804-71insTCGCCGT
XM_005250425.1:c.1804-72_1804-71insTCGCCGT	XP_005250482.1:n.1804-72_1804-71insTCGCCGT
XM_005250425.2:c.1804-72_1804-71insTCGCCGT	XP_005250482.1:n.1804-72_1804-71insTCGCCGT
XM_017012318.1:c.1726-72_1726-71insTCGCCGT	XP_016867807.1:n.1726-72_1726-71insTCGCCGT
NM_000441.2:c.1804-72_1804-71insTCGCCGT MANE Select	NP_000432.1:n.1804-72_1804-71insTCGCCGT