Canonical Allele Identifier: CA164227806

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1053293530
• gnomAD v3: 7-107709836-ATTTCT-A
• gnomAD v4: 7-107709836-ATTTCT-A
• MyVariant Identifiers: chr7:g.107350282_107350286del (hg19) ; chr7:g.107709837_107709841del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709843_107709847del , CM000669.2:g.107709843_107709847del	GRCh38
NC_000007.13:g.107350288_107350292del , CM000669.1:g.107350288_107350292del	GRCh37
NC_000007.12:g.107137524_107137528del	NCBI36
NG_008489.1:g.54209_54213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-211_2090-207del MANE Select	ENSP00000494017.1:n.2090-211_2090-207del
ENST00000644846.1:c.746-211_746-207del
ENST00000265715.7:c.2090-211_2090-207del	ENSP00000265715.3:n.2090-211_2090-207del
ENST00000492030.2:n.377-312_377-308del
NM_000441.1:c.2090-211_2090-207del	NP_000432.1:n.2090-211_2090-207del
XM_005250425.1:c.2090-211_2090-207del	XP_005250482.1:n.2090-211_2090-207del
XM_005250425.2:c.2090-211_2090-207del	XP_005250482.1:n.2090-211_2090-207del
XM_017012318.1:c.2012-211_2012-207del	XP_016867807.1:n.2012-211_2012-207del
NM_000441.2:c.2090-211_2090-207del MANE Select	NP_000432.1:n.2090-211_2090-207del