Canonical Allele Identifier: CA645586573
Gene: KERA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055982_91055983delinsAT , CM000674.2:g.91055982_91055983delinsAT GRCh38
NC_000012.11:g.91449759_91449760delinsAT , CM000674.1:g.91449759_91449760delinsAT GRCh37
NC_000012.10:g.89973890_89973891delinsAT NCBI36
NG_021223.1:g.7372_7373delinsAT , LRG_538:g.7372_7373delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.299_300delinsAT MANE Select ENSP00000266719.3:p.Ile100Asn
ENST00000266719.3:c.299_300delinsAT ENSP00000266719.3:p.Ile100Asn
NM_007035.3:c.299_300delinsAT , LRG_538t1:c.299_300delinsAT NP_008966.1:p.Ile100Asn
XM_011537781.1:c.299_300delinsAT XP_011536083.1:p.Ile100Asn
NM_007035.4:c.299_300delinsAT MANE Select NP_008966.1:p.Ile100Asn