Canonical Allele Identifier: CA1732748350

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690193_107690194delinsCT , CM000669.2:g.107690193_107690194delinsCT	GRCh38
NC_000007.13:g.107330638_107330639delinsCT , CM000669.1:g.107330638_107330639delinsCT	GRCh37
NC_000007.12:g.107117874_107117875delinsCT	NCBI36
NG_008489.1:g.34559_34560delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1219_1220delinsCT MANE Select	ENSP00000494017.1:p.Leu407=
ENST00000265715.7:c.1219_1220delinsCT	ENSP00000265715.3:p.Leu407=
NM_000441.1:c.1219_1220delinsCT	NP_000432.1:p.Leu407=
XM_005250425.1:c.1219_1220delinsCT	XP_005250482.1:p.Leu407=
XM_006716025.2:c.1219_1220delinsCT	XP_006716088.1:p.Leu407=
XM_005250425.2:c.1219_1220delinsCT	XP_005250482.1:p.Leu407=
XM_006716025.3:c.1219_1220delinsCT	XP_006716088.1:p.Leu407=
XM_017012318.1:c.1219_1220delinsCT	XP_016867807.1:p.Leu407=
NM_000441.2:c.1219_1220delinsCT MANE Select	NP_000432.1:p.Leu407=