Canonical Allele Identifier: CA1732751386

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107710170C= , CM000669.2:g.107710170C=	GRCh38
NC_000007.13:g.107350615C= , CM000669.1:g.107350615C=	GRCh37
NC_000007.12:g.107137851C=	NCBI36
NG_008489.1:g.54536C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2206C= MANE Select	ENSP00000494017.1:p.Gln736=
ENST00000644846.1:c.862C=
ENST00000265715.7:c.2206C=	ENSP00000265715.3:p.Gln736=
ENST00000492030.2:n.392C=
NM_000441.1:c.2206C=	NP_000432.1:p.Gln736=
XM_005250425.1:c.2206C=	XP_005250482.1:p.Gln736=
XM_005250425.2:c.2206C=	XP_005250482.1:p.Gln736=
XM_017012318.1:c.2128C=	XP_016867807.1:p.Gln710=
NM_000441.2:c.2206C= MANE Select	NP_000432.1:p.Gln736=