Canonical Allele Identifier: CA1732742071

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683561_107683562delinsAC , CM000669.2:g.107683561_107683562delinsAC	GRCh38
NC_000007.13:g.107324006_107324007delinsAC , CM000669.1:g.107324006_107324007delinsAC	GRCh37
NC_000007.12:g.107111242_107111243delinsAC	NCBI36
NG_008489.1:g.27927_27928delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1001+24_1001+25delinsAC MANE Select	ENSP00000494017.1:n.1001+24_1001+25delins...
ENST00000265715.7:c.1001+24_1001+25delinsAC	ENSP00000265715.3:n.1001+24_1001+25delins...
NM_000441.1:c.1001+24_1001+25delinsAC	NP_000432.1:n.1001+24_1001+25delinsAC
XM_005250425.1:c.1001+24_1001+25delinsAC	XP_005250482.1:n.1001+24_1001+25delinsAC
XM_006716025.2:c.1001+24_1001+25delinsAC	XP_006716088.1:n.1001+24_1001+25delinsAC
XM_005250425.2:c.1001+24_1001+25delinsAC	XP_005250482.1:n.1001+24_1001+25delinsAC
XM_006716025.3:c.1001+24_1001+25delinsAC	XP_006716088.1:n.1001+24_1001+25delinsAC
XM_017012318.1:c.1001+24_1001+25delinsAC	XP_016867807.1:n.1001+24_1001+25delinsAC
NM_000441.2:c.1001+24_1001+25delinsAC MANE Select	NP_000432.1:n.1001+24_1001+25delinsAC