Canonical Allele Identifier: CA457104128

Gene: SLC26A4 SLC26A4-AS1

Linked Data

• ClinVar Variation Id: 1508044
• ClinVar RCV Id: RCV002040317
• dbSNP Id: rs755036570
• gnomAD v2: 7-107302128-C-T
• gnomAD v4: 7-107661683-C-T
• MyVariant Identifiers: chr7:g.107302128C>T (hg19) ; chr7:g.107661683C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661683C>T , CM000669.2:g.107661683C>T	GRCh38
NC_000007.13:g.107302128C>T , CM000669.1:g.107302128C>T	GRCh37
NC_000007.12:g.107089364C>T	NCBI36
NG_008489.1:g.6049C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.42C>T (SLC26A4) MANE Select	ENSP00000494017.1:p.Pro14=
ENST00000265715.7:c.42C>T (SLC26A4)	ENSP00000265715.3:p.Pro14=
ENST00000440056.1:c.42C>T (SLC26A4)	ENSP00000394760.1:p.Pro14=
NM_000441.1:c.42C>T (SLC26A4)	NP_000432.1:p.Pro14=
NR_028137.1:n.116G>A (SLC26A4-AS1)
XM_005250425.1:c.42C>T (SLC26A4)	XP_005250482.1:p.Pro14=
XM_006716025.2:c.42C>T (SLC26A4)	XP_006716088.1:p.Pro14=
XM_005250425.2:c.42C>T (SLC26A4)	XP_005250482.1:p.Pro14=
XM_006716025.3:c.42C>T (SLC26A4)	XP_006716088.1:p.Pro14=
XM_017012318.1:c.42C>T (SLC26A4)	XP_016867807.1:p.Pro14=
NM_000441.2:c.42C>T (SLC26A4) MANE Select	NP_000432.1:p.Pro14=