Canonical Allele Identifier: CA2054259670
Gene: KERA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055556_91055557delinsCA , CM000674.2:g.91055556_91055557delinsCA GRCh38
NC_000012.11:g.91449333_91449334delinsCA , CM000674.1:g.91449333_91449334delinsCA GRCh37
NC_000012.10:g.89973464_89973465delinsCA NCBI36
NG_021223.1:g.7798_7799delinsTG , LRG_538:g.7798_7799delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000266719.4:c.725_726delinsTG MANE Select ENSP00000266719.3:p.Leu242=
ENST00000266719.3:c.725_726delinsTG ENSP00000266719.3:p.Leu242=
NM_007035.3:c.725_726delinsTG , LRG_538t1:c.725_726delinsTG NP_008966.1:p.Leu242=
XM_011537781.1:c.725_726delinsTG XP_011536083.1:p.Leu242=
NM_007035.4:c.725_726delinsTG MANE Select NP_008966.1:p.Leu242=