Canonical Allele Identifier: CA1732751187
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710069_107710070delinsAG , CM000669.2:g.107710069_107710070delinsAG GRCh38
NC_000007.13:g.107350514_107350515delinsAG , CM000669.1:g.107350514_107350515delinsAG GRCh37
NC_000007.12:g.107137750_107137751delinsAG NCBI36
NG_008489.1:g.54435_54436delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2105_2106delinsAG MANE Select ENSP00000494017.1:p.Lys702=
ENST00000644846.1:c.761_762delinsAG
ENST00000265715.7:c.2105_2106delinsAG ENSP00000265715.3:p.Lys702=
ENST00000492030.2:n.377-86_377-85delinsAG
NM_000441.1:c.2105_2106delinsAG NP_000432.1:p.Lys702=
XM_005250425.1:c.2105_2106delinsAG XP_005250482.1:p.Lys702=
XM_005250425.2:c.2105_2106delinsAG XP_005250482.1:p.Lys702=
XM_017012318.1:c.2027_2028delinsAG XP_016867807.1:p.Lys676=
NM_000441.2:c.2105_2106delinsAG MANE Select NP_000432.1:p.Lys702=