Canonical Allele Identifier: CA2054259577

Gene: KERA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91055359G= , CM000674.2:g.91055359G=	GRCh38
NC_000012.11:g.91449136G= , CM000674.1:g.91449136G=	GRCh37
NC_000012.10:g.89973267G=	NCBI36
NG_021223.1:g.7996C= , LRG_538:g.7996C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266719.4:c.886+37C= MANE Select	ENSP00000266719.3:n.886+37C=
ENST00000266719.3:c.886+37C=	ENSP00000266719.3:n.886+37C=
NM_007035.3:c.886+37C= , LRG_538t1:c.886+37C=	NP_008966.1:n.886+37C=
XM_011537781.1:c.886+37C=	XP_011536083.1:n.886+37C=
NM_007035.4:c.886+37C= MANE Select	NP_008966.1:n.886+37C=