Canonical Allele Identifier: CA386014362
Gene: KERA HGNC NCBI

Linked Data

dbSNP Id: rs1451070433

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055961T>C , CM000674.2:g.91055961T>C GRCh38
NC_000012.11:g.91449738T>C , CM000674.1:g.91449738T>C GRCh37
NC_000012.10:g.89973869T>C NCBI36
NG_021223.1:g.7394A>G , LRG_538:g.7394A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.321A>G MANE Select ENSP00000266719.3:p.Ile107Met
ENST00000266719.3:c.321A>G ENSP00000266719.3:p.Ile107Met
NM_007035.3:c.321A>G , LRG_538t1:c.321A>G NP_008966.1:p.Ile107Met
XM_011537781.1:c.321A>G XP_011536083.1:p.Ile107Met
NM_007035.4:c.321A>G MANE Select NP_008966.1:p.Ile107Met