Canonical Allele Identifier: CA2054259600
Gene: KERA HGNC NCBI

Linked Data

dbSNP Id: rs1878968228

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055394_91055397del , CM000674.2:g.91055394_91055397del GRCh38
NC_000012.11:g.91449171_91449174del , CM000674.1:g.91449171_91449174del GRCh37
NC_000012.10:g.89973302_89973305del NCBI36
NG_021223.1:g.7964_7967del , LRG_538:g.7964_7967del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.886+5_886+8del
ENST00000266719.3:c.886+5_886+8del
NM_007035.3:c.886+5_886+8del , LRG_538t1:c.886+5_886+8del
XM_011537781.1:c.886+5_886+8del
NM_007035.4:c.886+5_886+8del