Canonical Allele Identifier: CA386014018
Gene: KERA HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.91449581C>A (hg19) chr12:g.91055804C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055804C>A , CM000674.2:g.91055804C>A GRCh38
NC_000012.11:g.91449581C>A , CM000674.1:g.91449581C>A GRCh37
NC_000012.10:g.89973712C>A NCBI36
NG_021223.1:g.7551G>T , LRG_538:g.7551G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.478G>T MANE Select ENSP00000266719.3:p.Gly160Trp
ENST00000266719.3:c.478G>T ENSP00000266719.3:p.Gly160Trp
NM_007035.3:c.478G>T , LRG_538t1:c.478G>T NP_008966.1:p.Gly160Trp
XM_011537781.1:c.478G>T XP_011536083.1:p.Gly160Trp
NM_007035.4:c.478G>T MANE Select NP_008966.1:p.Gly160Trp
Search 100 bp 5'
Search 100 bp 3'