Canonical Allele Identifier: CA457103248

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107342367A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701922A>G , CM000669.2:g.107701922A>G	GRCh38
NC_000007.13:g.107342367A>G , CM000669.1:g.107342367A>G	GRCh37
NC_000007.12:g.107129603A>G	NCBI36
NG_008489.1:g.46288A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1899A>G MANE Select	ENSP00000494017.1:p.Glu633=
ENST00000644846.1:c.610A>G
ENST00000265715.7:c.1899A>G	ENSP00000265715.3:p.Glu633=
ENST00000492030.2:n.186A>G
NM_000441.1:c.1899A>G	NP_000432.1:p.Glu633=
XM_005250425.1:c.1899A>G	XP_005250482.1:p.Glu633=
XM_005250425.2:c.1899A>G	XP_005250482.1:p.Glu633=
XM_017012318.1:c.1821A>G	XP_016867807.1:p.Glu607=
NM_000441.2:c.1899A>G MANE Select	NP_000432.1:p.Glu633=