Canonical Allele Identifier: CA2054260265
Gene: KERA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91056011A= , CM000674.2:g.91056011A= GRCh38
NC_000012.11:g.91449788A= , CM000674.1:g.91449788A= GRCh37
NC_000012.10:g.89973919A= NCBI36
NG_021223.1:g.7344T= , LRG_538:g.7344T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.271T= MANE Select ENSP00000266719.3:p.Phe91=
ENST00000266719.3:c.271T= ENSP00000266719.3:p.Phe91=
NM_007035.3:c.271T= , LRG_538t1:c.271T= NP_008966.1:p.Phe91=
XM_011537781.1:c.271T= XP_011536083.1:p.Phe91=
NM_007035.4:c.271T= MANE Select NP_008966.1:p.Phe91=
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