Canonical Allele Identifier: CA386013908
Gene: KERA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055752T>G , CM000674.2:g.91055752T>G GRCh38
NC_000012.11:g.91449529T>G , CM000674.1:g.91449529T>G GRCh37
NC_000012.10:g.89973660T>G NCBI36
NG_021223.1:g.7603A>C , LRG_538:g.7603A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.530A>C MANE Select ENSP00000266719.3:p.Lys177Thr
ENST00000266719.3:c.530A>C ENSP00000266719.3:p.Lys177Thr
NM_007035.3:c.530A>C , LRG_538t1:c.530A>C NP_008966.1:p.Lys177Thr
XM_011537781.1:c.530A>C XP_011536083.1:p.Lys177Thr
NM_007035.4:c.530A>C MANE Select NP_008966.1:p.Lys177Thr