Canonical Allele Identifier: CA1105628237

Gene: SLC26A4

Linked Data

• gnomAD v3: 7-107675254-C-T
• gnomAD v4: 7-107675254-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107675254C>T , CM000669.2:g.107675254C>T	GRCh38
NC_000007.13:g.107315699C>T , CM000669.1:g.107315699C>T	GRCh37
NC_000007.12:g.107102935C>T	NCBI36
NG_008489.1:g.19620C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.765+145C>T MANE Select	ENSP00000494017.1:n.765+145C>T
ENST00000265715.7:c.765+145C>T	ENSP00000265715.3:n.765+145C>T
NM_000441.1:c.765+145C>T	NP_000432.1:n.765+145C>T
XM_005250425.1:c.765+145C>T	XP_005250482.1:n.765+145C>T
XM_006716025.2:c.765+145C>T	XP_006716088.1:n.765+145C>T
XM_005250425.2:c.765+145C>T	XP_005250482.1:n.765+145C>T
XM_006716025.3:c.765+145C>T	XP_006716088.1:n.765+145C>T
XM_017012318.1:c.765+145C>T	XP_016867807.1:n.765+145C>T
NM_000441.2:c.765+145C>T MANE Select	NP_000432.1:n.765+145C>T