Canonical Allele Identifier: CA1732742170

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683653_107683654delinsAT , CM000669.2:g.107683653_107683654delinsAT	GRCh38
NC_000007.13:g.107324098_107324099delinsAT , CM000669.1:g.107324098_107324099delinsAT	GRCh37
NC_000007.12:g.107111334_107111335delinsAT	NCBI36
NG_008489.1:g.28019_28020delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1001+116_1001+117delinsAT MANE Select	ENSP00000494017.1:n.1001+116_1001+117delinsAT
ENST00000265715.7:c.1001+116_1001+117delinsAT	ENSP00000265715.3:n.1001+116_1001+117delinsAT
NM_000441.1:c.1001+116_1001+117delinsAT	NP_000432.1:n.1001+116_1001+117delinsAT
XM_005250425.1:c.1001+116_1001+117delinsAT	XP_005250482.1:n.1001+116_1001+117delinsAT
XM_006716025.2:c.1001+116_1001+117delinsAT	XP_006716088.1:n.1001+116_1001+117delinsAT
XM_005250425.2:c.1001+116_1001+117delinsAT	XP_005250482.1:n.1001+116_1001+117delinsAT
XM_006716025.3:c.1001+116_1001+117delinsAT	XP_006716088.1:n.1001+116_1001+117delinsAT
XM_017012318.1:c.1001+116_1001+117delinsAT	XP_016867807.1:n.1001+116_1001+117delinsAT
NM_000441.2:c.1001+116_1001+117delinsAT MANE Select	NP_000432.1:n.1001+116_1001+117delinsAT