Canonical Allele Identifier: CA1105627658

Gene: SLC26A4

Linked Data

• gnomAD v3: 7-107674167-C-CTTTTTTTTTT
• gnomAD v4: 7-107674167-C-CTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107674171_107674172insTTTTTTTTTT , CM000669.2:g.107674171_107674172insTTTTTTTTTT	GRCh38
NC_000007.13:g.107314616_107314617insTTTTTTTTTT , CM000669.1:g.107314616_107314617insTTTTTTTTTT	GRCh37
NC_000007.12:g.107101852_107101853insTTTTTTTTTT	NCBI36
NG_008489.1:g.18537_18538insTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.423_424insTTTTTTTTTT MANE Select	ENSP00000494017.1:p.Pro142PhefsTer?
ENST00000265715.7:c.423_424insTTTTTTTTTT	ENSP00000265715.3:p.Pro142PhefsTer?
NM_000441.1:c.423_424insTTTTTTTTTT	NP_000432.1:p.Pro142PhefsTer?
XM_005250425.1:c.423_424insTTTTTTTTTT	XP_005250482.1:p.Pro142PhefsTer?
XM_006716025.2:c.423_424insTTTTTTTTTT	XP_006716088.1:p.Pro142PhefsTer?
XM_005250425.2:c.423_424insTTTTTTTTTT	XP_005250482.1:p.Pro142PhefsTer?
XM_006716025.3:c.423_424insTTTTTTTTTT	XP_006716088.1:p.Pro142PhefsTer?
XM_017012318.1:c.423_424insTTTTTTTTTT	XP_016867807.1:p.Pro142PhefsTer?
NM_000441.2:c.423_424insTTTTTTTTTT MANE Select	NP_000432.1:p.Pro142PhefsTer?