Canonical Allele Identifier: CA386013716
Gene: KERA HGNC NCBI

Linked Data

ClinVar Variation Id: 2227124
ClinVar RCV Id: RCV002678719

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055665T>A , CM000674.2:g.91055665T>A GRCh38
NC_000012.11:g.91449442T>A , CM000674.1:g.91449442T>A GRCh37
NC_000012.10:g.89973573T>A NCBI36
NG_021223.1:g.7690A>T , LRG_538:g.7690A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266719.4:c.617A>T MANE Select ENSP00000266719.3:p.Asn206Ile
ENST00000266719.3:c.617A>T ENSP00000266719.3:p.Asn206Ile
NM_007035.3:c.617A>T , LRG_538t1:c.617A>T NP_008966.1:p.Asn206Ile
XM_011537781.1:c.617A>T XP_011536083.1:p.Asn206Ile
NM_007035.4:c.617A>T MANE Select NP_008966.1:p.Asn206Ile