Canonical Allele Identifier: CA2054259649
Gene: KERA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055515G= , CM000674.2:g.91055515G= GRCh38
NC_000012.11:g.91449292G= , CM000674.1:g.91449292G= GRCh37
NC_000012.10:g.89973423G= NCBI36
NG_021223.1:g.7840C= , LRG_538:g.7840C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.767C= MANE Select ENSP00000266719.3:p.Ser256=
ENST00000266719.3:c.767C= ENSP00000266719.3:p.Ser256=
NM_007035.3:c.767C= , LRG_538t1:c.767C= NP_008966.1:p.Ser256=
XM_011537781.1:c.767C= XP_011536083.1:p.Ser256=
NM_007035.4:c.767C= MANE Select NP_008966.1:p.Ser256=
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