Canonical Allele Identifier: CA386013564
Gene: KERA HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.91449374G>T (hg19) chr12:g.91055597G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055597G>T , CM000674.2:g.91055597G>T GRCh38
NC_000012.11:g.91449374G>T , CM000674.1:g.91449374G>T GRCh37
NC_000012.10:g.89973505G>T NCBI36
NG_021223.1:g.7758C>A , LRG_538:g.7758C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.685C>A MANE Select ENSP00000266719.3:p.Pro229Thr
ENST00000266719.3:c.685C>A ENSP00000266719.3:p.Pro229Thr
NM_007035.3:c.685C>A , LRG_538t1:c.685C>A NP_008966.1:p.Pro229Thr
XM_011537781.1:c.685C>A XP_011536083.1:p.Pro229Thr
NM_007035.4:c.685C>A MANE Select NP_008966.1:p.Pro229Thr
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