Canonical Allele Identifier: CA2054260137
Gene: KERA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055953T= , CM000674.2:g.91055953T= GRCh38
NC_000012.11:g.91449730T= , CM000674.1:g.91449730T= GRCh37
NC_000012.10:g.89973861T= NCBI36
NG_021223.1:g.7402A= , LRG_538:g.7402A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.329A= MANE Select ENSP00000266719.3:p.Tyr110=
ENST00000266719.3:c.329A= ENSP00000266719.3:p.Tyr110=
NM_007035.3:c.329A= , LRG_538t1:c.329A= NP_008966.1:p.Tyr110=
XM_011537781.1:c.329A= XP_011536083.1:p.Tyr110=
NM_007035.4:c.329A= MANE Select NP_008966.1:p.Tyr110=
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