Canonical Allele Identifier: CA2054259722

Gene: KERA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91055676A= , CM000674.2:g.91055676A=	GRCh38
NC_000012.11:g.91449453A= , CM000674.1:g.91449453A=	GRCh37
NC_000012.10:g.89973584A=	NCBI36
NG_021223.1:g.7679T= , LRG_538:g.7679T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000266719.4:c.606T= MANE Select	ENSP00000266719.3:p.Asn202=
ENST00000266719.3:c.606T=	ENSP00000266719.3:p.Asn202=
NM_007035.3:c.606T= , LRG_538t1:c.606T=	NP_008966.1:p.Asn202=
XM_011537781.1:c.606T=	XP_011536083.1:p.Asn202=
NM_007035.4:c.606T= MANE Select	NP_008966.1:p.Asn202=