Canonical Allele Identifier: CA386013429
Gene: KERA HGNC NCBI

Linked Data

dbSNP Id: rs1157805641

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055534A>G , CM000674.2:g.91055534A>G GRCh38
NC_000012.11:g.91449311A>G , CM000674.1:g.91449311A>G GRCh37
NC_000012.10:g.89973442A>G NCBI36
NG_021223.1:g.7821T>C , LRG_538:g.7821T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.748T>C MANE Select ENSP00000266719.3:p.Ser250Pro
ENST00000266719.3:c.748T>C ENSP00000266719.3:p.Ser250Pro
NM_007035.3:c.748T>C , LRG_538t1:c.748T>C NP_008966.1:p.Ser250Pro
XM_011537781.1:c.748T>C XP_011536083.1:p.Ser250Pro
NM_007035.4:c.748T>C MANE Select NP_008966.1:p.Ser250Pro