Canonical Allele Identifier: CA386013328

Gene: KERA

Linked Data

• MyVariant Identifiers: chr12:g.91449262T>A (hg19) ; chr12:g.91055485T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91055485T>A , CM000674.2:g.91055485T>A	GRCh38
NC_000012.11:g.91449262T>A , CM000674.1:g.91449262T>A	GRCh37
NC_000012.10:g.89973393T>A	NCBI36
NG_021223.1:g.7870A>T , LRG_538:g.7870A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266719.4:c.797A>T MANE Select	ENSP00000266719.3:p.Asp266Val
ENST00000266719.3:c.797A>T	ENSP00000266719.3:p.Asp266Val
NM_007035.3:c.797A>T , LRG_538t1:c.797A>T	NP_008966.1:p.Asp266Val
XM_011537781.1:c.797A>T	XP_011536083.1:p.Asp266Val
NM_007035.4:c.797A>T MANE Select	NP_008966.1:p.Asp266Val