Canonical Allele Identifier: CA577198857

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1188177180
• gnomAD v2: 7-107314531-AT-A
• gnomAD v3: 7-107674086-AT-A
• gnomAD v4: 7-107674086-AT-A
• MyVariant Identifiers: chr7:g.107314532del (hg19) ; chr7:g.107674087del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107674092del , CM000669.2:g.107674092del	GRCh38
NC_000007.13:g.107314537del , CM000669.1:g.107314537del	GRCh37
NC_000007.12:g.107101773del	NCBI36
NG_008489.1:g.18458del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.416-72del MANE Select	ENSP00000494017.1:n.416-72del
ENST00000265715.7:c.416-72del	ENSP00000265715.3:n.416-72del
NM_000441.1:c.416-72del	NP_000432.1:n.416-72del
XM_005250425.1:c.416-72del	XP_005250482.1:n.416-72del
XM_006716025.2:c.416-72del	XP_006716088.1:n.416-72del
XM_005250425.2:c.416-72del	XP_005250482.1:n.416-72del
XM_006716025.3:c.416-72del	XP_006716088.1:n.416-72del
XM_017012318.1:c.416-72del	XP_016867807.1:n.416-72del
NM_000441.2:c.416-72del MANE Select	NP_000432.1:n.416-72del