Canonical Allele Identifier: CA1732758396

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701125_107701128delinsTATA , CM000669.2:g.107701125_107701128delinsTATA	GRCh38
NC_000007.13:g.107341570_107341573delinsTATA , CM000669.1:g.107341570_107341573delinsTATA	GRCh37
NC_000007.12:g.107128806_107128809delinsTATA	NCBI36
NG_008489.1:g.45491_45494delinsTATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1732_1735delinsTATA MANE Select	ENSP00000494017.1:p.Tyr578=
ENST00000644846.1:c.443_446delinsTATA
ENST00000265715.7:c.1732_1735delinsTATA	ENSP00000265715.3:p.Tyr578=
ENST00000480841.5:n.581_584delinsTATA
ENST00000492030.2:n.91-702_91-699delinsTATA
NM_000441.1:c.1732_1735delinsTATA	NP_000432.1:p.Tyr578=
XM_005250425.1:c.1732_1735delinsTATA	XP_005250482.1:p.Tyr578=
XM_005250425.2:c.1732_1735delinsTATA	XP_005250482.1:p.Tyr578=
XM_017012318.1:c.1654_1657delinsTATA	XP_016867807.1:p.Tyr552=
NM_000441.2:c.1732_1735delinsTATA MANE Select	NP_000432.1:p.Tyr578=