Canonical Allele Identifier: CA386014453
Gene: KERA HGNC NCBI

Linked Data

dbSNP Id: rs991300088

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91056002C>G , CM000674.2:g.91056002C>G GRCh38
NC_000012.11:g.91449779C>G , CM000674.1:g.91449779C>G GRCh37
NC_000012.10:g.89973910C>G NCBI36
NG_021223.1:g.7353G>C , LRG_538:g.7353G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.280G>C MANE Select ENSP00000266719.3:p.Ala94Pro
ENST00000266719.3:c.280G>C ENSP00000266719.3:p.Ala94Pro
NM_007035.3:c.280G>C , LRG_538t1:c.280G>C NP_008966.1:p.Ala94Pro
XM_011537781.1:c.280G>C XP_011536083.1:p.Ala94Pro
NM_007035.4:c.280G>C MANE Select NP_008966.1:p.Ala94Pro