Canonical Allele Identifier: CA1732747252

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107675232G= , CM000669.2:g.107675232G=	GRCh38
NC_000007.13:g.107315677G= , CM000669.1:g.107315677G=	GRCh37
NC_000007.12:g.107102913G=	NCBI36
NG_008489.1:g.19598G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.765+123G= MANE Select	ENSP00000494017.1:n.765+123G=
ENST00000265715.7:c.765+123G=	ENSP00000265715.3:n.765+123G=
NM_000441.1:c.765+123G=	NP_000432.1:n.765+123G=
XM_005250425.1:c.765+123G=	XP_005250482.1:n.765+123G=
XM_006716025.2:c.765+123G=	XP_006716088.1:n.765+123G=
XM_005250425.2:c.765+123G=	XP_005250482.1:n.765+123G=
XM_006716025.3:c.765+123G=	XP_006716088.1:n.765+123G=
XM_017012318.1:c.765+123G=	XP_016867807.1:n.765+123G=
NM_000441.2:c.765+123G= MANE Select	NP_000432.1:n.765+123G=