Canonical Allele Identifier: CA2620149229
Gene: KERA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055377T>G , CM000674.2:g.91055377T>G GRCh38
NC_000012.11:g.91449154T>G , CM000674.1:g.91449154T>G GRCh37
NC_000012.10:g.89973285T>G NCBI36
NG_021223.1:g.7978A>C , LRG_538:g.7978A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.886+19A>C MANE Select ENSP00000266719.3:n.886+19A>C
ENST00000266719.3:c.886+19A>C ENSP00000266719.3:n.886+19A>C
NM_007035.3:c.886+19A>C , LRG_538t1:c.886+19A>C NP_008966.1:n.886+19A>C
XM_011537781.1:c.886+19A>C XP_011536083.1:n.886+19A>C
NM_007035.4:c.886+19A>C MANE Select NP_008966.1:n.886+19A>C