Canonical Allele Identifier: CA2054259729
Gene: KERA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055685C= , CM000674.2:g.91055685C= GRCh38
NC_000012.11:g.91449462C= , CM000674.1:g.91449462C= GRCh37
NC_000012.10:g.89973593C= NCBI36
NG_021223.1:g.7670G= , LRG_538:g.7670G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.597G= MANE Select ENSP00000266719.3:p.Met199=
ENST00000266719.3:c.597G= ENSP00000266719.3:p.Met199=
NM_007035.3:c.597G= , LRG_538t1:c.597G= NP_008966.1:p.Met199=
XM_011537781.1:c.597G= XP_011536083.1:p.Met199=
NM_007035.4:c.597G= MANE Select NP_008966.1:p.Met199=