Canonical Allele Identifier: CA2620149235
Gene: KERA HGNC NCBI

Linked Data

gnomAD v4: 12-91055492-TTGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055497_91055499del , CM000674.2:g.91055497_91055499del GRCh38
NC_000012.11:g.91449274_91449276del , CM000674.1:g.91449274_91449276del GRCh37
NC_000012.10:g.89973405_89973407del NCBI36
NG_021223.1:g.7860_7862del , LRG_538:g.7860_7862del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.787_789del MANE Select ENSP00000266719.3:p.Ser263del
ENST00000266719.3:c.787_789del ENSP00000266719.3:p.Ser263del
NM_007035.3:c.787_789del , LRG_538t1:c.787_789del NP_008966.1:p.Ser263del
XM_011537781.1:c.787_789del XP_011536083.1:p.Ser263del
NM_007035.4:c.787_789del MANE Select NP_008966.1:p.Ser263del
Search 100 bp 5'
Search 100 bp 3'