Canonical Allele Identifier: CA1732747185

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107675115_107675116delinsTG , CM000669.2:g.107675115_107675116delinsTG	GRCh38
NC_000007.13:g.107315560_107315561delinsTG , CM000669.1:g.107315560_107315561delinsTG	GRCh37
NC_000007.12:g.107102796_107102797delinsTG	NCBI36
NG_008489.1:g.19481_19482delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.765+6_765+7delinsTG MANE Select	ENSP00000494017.1:n.765+6_765+7delinsTG
ENST00000265715.7:c.765+6_765+7delinsTG	ENSP00000265715.3:n.765+6_765+7delinsTG
NM_000441.1:c.765+6_765+7delinsTG	NP_000432.1:n.765+6_765+7delinsTG
XM_005250425.1:c.765+6_765+7delinsTG	XP_005250482.1:n.765+6_765+7delinsTG
XM_006716025.2:c.765+6_765+7delinsTG	XP_006716088.1:n.765+6_765+7delinsTG
XM_005250425.2:c.765+6_765+7delinsTG	XP_005250482.1:n.765+6_765+7delinsTG
XM_006716025.3:c.765+6_765+7delinsTG	XP_006716088.1:n.765+6_765+7delinsTG
XM_017012318.1:c.765+6_765+7delinsTG	XP_016867807.1:n.765+6_765+7delinsTG
NM_000441.2:c.765+6_765+7delinsTG MANE Select	NP_000432.1:n.765+6_765+7delinsTG