Canonical Allele Identifier: CA2777354948

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107689253_107689254insCACACCCAAC , CM000669.2:g.107689253_107689254insCACACCCAAC	GRCh38
NC_000007.13:g.107329698_107329699insCACACCCAAC , CM000669.1:g.107329698_107329699insCACACCCAAC	GRCh37
NC_000007.12:g.107116934_107116935insCACACCCAAC	NCBI36
NG_008489.1:g.33619_33620insCACACCCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1149+53_1149+54insCACACCCAAC MANE Select	ENSP00000494017.1:n.1149+53_1149+54insCACACCCAAC
ENST00000265715.7:c.1149+53_1149+54insCACACCCAAC	ENSP00000265715.3:n.1149+53_1149+54insCACACCCAAC
NM_000441.1:c.1149+53_1149+54insCACACCCAAC	NP_000432.1:n.1149+53_1149+54insCACACCCAAC
XM_005250425.1:c.1149+53_1149+54insCACACCCAAC	XP_005250482.1:n.1149+53_1149+54insCACACCCAAC
XM_006716025.2:c.1149+53_1149+54insCACACCCAAC	XP_006716088.1:n.1149+53_1149+54insCACACCCAAC
XM_005250425.2:c.1149+53_1149+54insCACACCCAAC	XP_005250482.1:n.1149+53_1149+54insCACACCCAAC
XM_006716025.3:c.1149+53_1149+54insCACACCCAAC	XP_006716088.1:n.1149+53_1149+54insCACACCCAAC
XM_017012318.1:c.1149+53_1149+54insCACACCCAAC	XP_016867807.1:n.1149+53_1149+54insCACACCCAAC
NM_000441.2:c.1149+53_1149+54insCACACCCAAC MANE Select	NP_000432.1:n.1149+53_1149+54insCACACCCAAC