Canonical Allele Identifier: CA1105620942

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1791892146
• gnomAD v3: 7-107701749-CTT-C
• gnomAD v4: 7-107701749-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701752_107701753del , CM000669.2:g.107701752_107701753del	GRCh38
NC_000007.13:g.107342197_107342198del , CM000669.1:g.107342197_107342198del	GRCh37
NC_000007.12:g.107129433_107129434del	NCBI36
NG_008489.1:g.46118_46119del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1804-75_1804-74del MANE Select	ENSP00000494017.1:n.1804-75_1804-74del
ENST00000644846.1:c.515-75_515-74del
ENST00000265715.7:c.1804-75_1804-74del	ENSP00000265715.3:n.1804-75_1804-74del
ENST00000480841.5:n.653-75_653-74del
ENST00000492030.2:n.91-75_91-74del
NM_000441.1:c.1804-75_1804-74del	NP_000432.1:n.1804-75_1804-74del
XM_005250425.1:c.1804-75_1804-74del	XP_005250482.1:n.1804-75_1804-74del
XM_005250425.2:c.1804-75_1804-74del	XP_005250482.1:n.1804-75_1804-74del
XM_017012318.1:c.1726-75_1726-74del	XP_016867807.1:n.1726-75_1726-74del
NM_000441.2:c.1804-75_1804-74del MANE Select	NP_000432.1:n.1804-75_1804-74del