Canonical Allele Identifier: CA1732747436

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107689238_107689239delinsTG , CM000669.2:g.107689238_107689239delinsTG	GRCh38
NC_000007.13:g.107329683_107329684delinsTG , CM000669.1:g.107329683_107329684delinsTG	GRCh37
NC_000007.12:g.107116919_107116920delinsTG	NCBI36
NG_008489.1:g.33604_33605delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1149+38_1149+39delinsTG MANE Select	ENSP00000494017.1:n.1149+38_1149+39delinsTG
ENST00000265715.7:c.1149+38_1149+39delinsTG	ENSP00000265715.3:n.1149+38_1149+39delinsTG
NM_000441.1:c.1149+38_1149+39delinsTG	NP_000432.1:n.1149+38_1149+39delinsTG
XM_005250425.1:c.1149+38_1149+39delinsTG	XP_005250482.1:n.1149+38_1149+39delinsTG
XM_006716025.2:c.1149+38_1149+39delinsTG	XP_006716088.1:n.1149+38_1149+39delinsTG
XM_005250425.2:c.1149+38_1149+39delinsTG	XP_005250482.1:n.1149+38_1149+39delinsTG
XM_006716025.3:c.1149+38_1149+39delinsTG	XP_006716088.1:n.1149+38_1149+39delinsTG
XM_017012318.1:c.1149+38_1149+39delinsTG	XP_016867807.1:n.1149+38_1149+39delinsTG
NM_000441.2:c.1149+38_1149+39delinsTG MANE Select	NP_000432.1:n.1149+38_1149+39delinsTG