Canonical Allele Identifier: CA164223360

Gene: SLC26A3

Linked Data

• dbSNP Id: rs891160551
• gnomAD v3: 7-107767701-AAG-A
• gnomAD v4: 7-107767701-AAG-A
• MyVariant Identifiers: chr7:g.107408147_107408148del (hg19) ; chr7:g.107767702_107767703del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107767705_107767706del , CM000669.2:g.107767705_107767706del	GRCh38
NC_000007.13:g.107408150_107408151del , CM000669.1:g.107408150_107408151del	GRCh37
NC_000007.12:g.107195386_107195387del	NCBI36
NG_008046.1:g.40531_40532del , LRG_683:g.40531_40532del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340010.10:c.2206-59_2206-58del MANE Select	ENSP00000345873.5:n.2206-59_2206-58del
ENST00000340010.9:c.2206-59_2206-58del	ENSP00000345873.5:n.2206-59_2206-58del
ENST00000379083.7:c.*1763-59_*1763-58del	ENSP00000368375.3:n.*1763-59_*1763-58del
NM_000111.2:c.2206-59_2206-58del , LRG_683t1:c.2206-59_2206-58del	NP_000102.1:n.2206-59_2206-58del
XM_011515867.1:c.2206-59_2206-58del	XP_011514169.1:n.2206-59_2206-58del
NM_000111.3:c.2206-59_2206-58del MANE Select	NP_000102.1:n.2206-59_2206-58del