Canonical Allele Identifier: CA2054259735
Gene: KERA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055686A= , CM000674.2:g.91055686A= GRCh38
NC_000012.11:g.91449463A= , CM000674.1:g.91449463A= GRCh37
NC_000012.10:g.89973594A= NCBI36
NG_021223.1:g.7669T= , LRG_538:g.7669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.596T= MANE Select ENSP00000266719.3:p.Met199=
ENST00000266719.3:c.596T= ENSP00000266719.3:p.Met199=
NM_007035.3:c.596T= , LRG_538t1:c.596T= NP_008966.1:p.Met199=
XM_011537781.1:c.596T= XP_011536083.1:p.Met199=
NM_007035.4:c.596T= MANE Select NP_008966.1:p.Met199=