Canonical Allele Identifier: CA481306496

Gene: KERA

Linked Data

• MyVariant Identifiers: chr12:g.91449276T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91055499T>A , CM000674.2:g.91055499T>A	GRCh38
NC_000012.11:g.91449276T>A , CM000674.1:g.91449276T>A	GRCh37
NC_000012.10:g.89973407T>A	NCBI36
NG_021223.1:g.7856A>T , LRG_538:g.7856A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266719.4:c.783A>T MANE Select	ENSP00000266719.3:p.Val261=
ENST00000266719.3:c.783A>T	ENSP00000266719.3:p.Val261=
NM_007035.3:c.783A>T , LRG_538t1:c.783A>T	NP_008966.1:p.Val261=
XM_011537781.1:c.783A>T	XP_011536083.1:p.Val261=
NM_007035.4:c.783A>T MANE Select	NP_008966.1:p.Val261=