Canonical Allele Identifier: CA2054260035
Gene: KERA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055910G= , CM000674.2:g.91055910G= GRCh38
NC_000012.11:g.91449687G= , CM000674.1:g.91449687G= GRCh37
NC_000012.10:g.89973818G= NCBI36
NG_021223.1:g.7445C= , LRG_538:g.7445C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.372C= MANE Select ENSP00000266719.3:p.Leu124=
ENST00000266719.3:c.372C= ENSP00000266719.3:p.Leu124=
NM_007035.3:c.372C= , LRG_538t1:c.372C= NP_008966.1:p.Leu124=
XM_011537781.1:c.372C= XP_011536083.1:p.Leu124=
NM_007035.4:c.372C= MANE Select NP_008966.1:p.Leu124=