Canonical Allele Identifier: CA2054259599

Gene: KERA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91055387_91055391delinsGTTAC , CM000674.2:g.91055387_91055391delinsGTTAC	GRCh38
NC_000012.11:g.91449164_91449168delinsGTTAC , CM000674.1:g.91449164_91449168delinsGTTAC	GRCh37
NC_000012.10:g.89973295_89973299delinsGTTAC	NCBI36
NG_021223.1:g.7964_7968delinsGTAAC , LRG_538:g.7964_7968delinsGTAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266719.4:c.886+5_886+9delinsGTAAC MANE Select	ENSP00000266719.3:n.886+5_886+9delinsGTAAC
ENST00000266719.3:c.886+5_886+9delinsGTAAC	ENSP00000266719.3:n.886+5_886+9delinsGTAAC
NM_007035.3:c.886+5_886+9delinsGTAAC , LRG_538t1:c.886+5_886+9delinsGTAAC	NP_008966.1:n.886+5_886+9delinsGTAAC
XM_011537781.1:c.886+5_886+9delinsGTAAC	XP_011536083.1:n.886+5_886+9delinsGTAAC
NM_007035.4:c.886+5_886+9delinsGTAAC MANE Select	NP_008966.1:n.886+5_886+9delinsGTAAC