Canonical Allele Identifier: CA481306994

Gene: KERA

Linked Data

• MyVariant Identifiers: chr12:g.91449774G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91055997G>A , CM000674.2:g.91055997G>A	GRCh38
NC_000012.11:g.91449774G>A , CM000674.1:g.91449774G>A	GRCh37
NC_000012.10:g.89973905G>A	NCBI36
NG_021223.1:g.7358C>T , LRG_538:g.7358C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266719.4:c.285C>T MANE Select	ENSP00000266719.3:p.Thr95=
ENST00000266719.3:c.285C>T	ENSP00000266719.3:p.Thr95=
NM_007035.3:c.285C>T , LRG_538t1:c.285C>T	NP_008966.1:p.Thr95=
XM_011537781.1:c.285C>T	XP_011536083.1:p.Thr95=
NM_007035.4:c.285C>T MANE Select	NP_008966.1:p.Thr95=