Canonical Allele Identifier: CA2054259905
Gene: KERA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055794C= , CM000674.2:g.91055794C= GRCh38
NC_000012.11:g.91449571C= , CM000674.1:g.91449571C= GRCh37
NC_000012.10:g.89973702C= NCBI36
NG_021223.1:g.7561G= , LRG_538:g.7561G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.488G= MANE Select ENSP00000266719.3:p.Ser163=
ENST00000266719.3:c.488G= ENSP00000266719.3:p.Ser163=
NM_007035.3:c.488G= , LRG_538t1:c.488G= NP_008966.1:p.Ser163=
XM_011537781.1:c.488G= XP_011536083.1:p.Ser163=
NM_007035.4:c.488G= MANE Select NP_008966.1:p.Ser163=