Canonical Allele Identifier: CA386013722
Gene: KERA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055668C>A , CM000674.2:g.91055668C>A GRCh38
NC_000012.11:g.91449445C>A , CM000674.1:g.91449445C>A GRCh37
NC_000012.10:g.89973576C>A NCBI36
NG_021223.1:g.7687G>T , LRG_538:g.7687G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266719.4:c.614G>T MANE Select ENSP00000266719.3:p.Arg205Met
ENST00000266719.3:c.614G>T ENSP00000266719.3:p.Arg205Met
NM_007035.3:c.614G>T , LRG_538t1:c.614G>T NP_008966.1:p.Arg205Met
XM_011537781.1:c.614G>T XP_011536083.1:p.Arg205Met
NM_007035.4:c.614G>T MANE Select NP_008966.1:p.Arg205Met