Canonical Allele Identifier: CA2054259916
Gene: KERA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055801T= , CM000674.2:g.91055801T= GRCh38
NC_000012.11:g.91449578T= , CM000674.1:g.91449578T= GRCh37
NC_000012.10:g.89973709T= NCBI36
NG_021223.1:g.7554A= , LRG_538:g.7554A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.481A= MANE Select ENSP00000266719.3:p.Thr161=
ENST00000266719.3:c.481A= ENSP00000266719.3:p.Thr161=
NM_007035.3:c.481A= , LRG_538t1:c.481A= NP_008966.1:p.Thr161=
XM_011537781.1:c.481A= XP_011536083.1:p.Thr161=
NM_007035.4:c.481A= MANE Select NP_008966.1:p.Thr161=