Canonical Allele Identifier: CA1732727702

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107662007G= , CM000669.2:g.107662007G=	GRCh38
NC_000007.13:g.107302452G= , CM000669.1:g.107302452G=	GRCh37
NC_000007.12:g.107089688G=	NCBI36
NG_008489.1:g.6373G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+202G= MANE Select	ENSP00000494017.1:n.164+202G=
ENST00000265715.7:c.164+202G=	ENSP00000265715.3:n.164+202G=
ENST00000440056.1:c.164+202G=	ENSP00000394760.1:n.164+202G=
NM_000441.1:c.164+202G=	NP_000432.1:n.164+202G=
XM_005250425.1:c.164+202G=	XP_005250482.1:n.164+202G=
XM_006716025.2:c.164+202G=	XP_006716088.1:n.164+202G=
XM_005250425.2:c.164+202G=	XP_005250482.1:n.164+202G=
XM_006716025.3:c.164+202G=	XP_006716088.1:n.164+202G=
XM_017012318.1:c.164+202G=	XP_016867807.1:n.164+202G=
NM_000441.2:c.164+202G= MANE Select	NP_000432.1:n.164+202G=