Canonical Allele Identifier: CA386013487
Gene: KERA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055561A>C , CM000674.2:g.91055561A>C GRCh38
NC_000012.11:g.91449338A>C , CM000674.1:g.91449338A>C GRCh37
NC_000012.10:g.89973469A>C NCBI36
NG_021223.1:g.7794T>G , LRG_538:g.7794T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.721T>G MANE Select ENSP00000266719.3:p.Phe241Val
ENST00000266719.3:c.721T>G ENSP00000266719.3:p.Phe241Val
NM_007035.3:c.721T>G , LRG_538t1:c.721T>G NP_008966.1:p.Phe241Val
XM_011537781.1:c.721T>G XP_011536083.1:p.Phe241Val
NM_007035.4:c.721T>G MANE Select NP_008966.1:p.Phe241Val