Canonical Allele Identifier: CA2777354941
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689250_107689251insCC , CM000669.2:g.107689250_107689251insCC GRCh38
NC_000007.13:g.107329695_107329696insCC , CM000669.1:g.107329695_107329696insCC GRCh37
NC_000007.12:g.107116931_107116932insCC NCBI36
NG_008489.1:g.33616_33617insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+50_1149+51insCC MANE Select ENSP00000494017.1:n.1149+50_1149+51insCC
ENST00000265715.7:c.1149+50_1149+51insCC ENSP00000265715.3:n.1149+50_1149+51insCC
NM_000441.1:c.1149+50_1149+51insCC NP_000432.1:n.1149+50_1149+51insCC
XM_005250425.1:c.1149+50_1149+51insCC XP_005250482.1:n.1149+50_1149+51insCC
XM_006716025.2:c.1149+50_1149+51insCC XP_006716088.1:n.1149+50_1149+51insCC
XM_005250425.2:c.1149+50_1149+51insCC XP_005250482.1:n.1149+50_1149+51insCC
XM_006716025.3:c.1149+50_1149+51insCC XP_006716088.1:n.1149+50_1149+51insCC
XM_017012318.1:c.1149+50_1149+51insCC XP_016867807.1:n.1149+50_1149+51insCC
NM_000441.2:c.1149+50_1149+51insCC MANE Select NP_000432.1:n.1149+50_1149+51insCC