Canonical Allele Identifier: CA1732753007

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695900_107695903delinsTATA , CM000669.2:g.107695900_107695903delinsTATA	GRCh38
NC_000007.13:g.107336345_107336348delinsTATA , CM000669.1:g.107336345_107336348delinsTATA	GRCh37
NC_000007.12:g.107123581_107123584delinsTATA	NCBI36
NG_008489.1:g.40266_40269delinsTATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-33_1438-30delinsTATA MANE Select	ENSP00000494017.1:n.1438-33_1438-30delins...
ENST00000644846.1:c.149-33_149-30delinsTATA
ENST00000265715.7:c.1438-33_1438-30delinsTATA	ENSP00000265715.3:n.1438-33_1438-30delins...
ENST00000460748.1:n.541-33_541-30delinsTATA
ENST00000477350.5:n.285-33_285-30delinsTATA
ENST00000480841.5:n.287-33_287-30delinsTATA
ENST00000497446.5:n.453-33_453-30delinsTATA
NM_000441.1:c.1438-33_1438-30delinsTATA	NP_000432.1:n.1438-33_1438-30delinsTATA
XM_005250425.1:c.1438-33_1438-30delinsTATA	XP_005250482.1:n.1438-33_1438-30delinsTAT...
XM_005250425.2:c.1438-33_1438-30delinsTATA	XP_005250482.1:n.1438-33_1438-30delinsTAT...
XM_017012318.1:c.1360-33_1360-30delinsTATA	XP_016867807.1:n.1360-33_1360-30delinsTAT...
NM_000441.2:c.1438-33_1438-30delinsTATA MANE Select	NP_000432.1:n.1438-33_1438-30delinsTATA