Canonical Allele Identifier: CA480069768

Gene: KRT5

Linked Data

• MyVariant Identifiers: chr12:g.52910567C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516783C>T , CM000674.2:g.52516783C>T	GRCh38
NC_000012.11:g.52910567C>T , CM000674.1:g.52910567C>T	GRCh37
NC_000012.10:g.51196834C>T	NCBI36
NG_008297.1:g.8677G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1293G>A MANE Select	ENSP00000252242.4:p.Lys431=
ENST00000252242.8:c.1293G>A	ENSP00000252242.4:p.Lys431=
ENST00000547890.5:n.671G>A
ENST00000548409.5:c.415G>A
ENST00000549511.5:n.500G>A
ENST00000552629.5:n.1391G>A
NM_000424.3:c.1293G>A	NP_000415.2:p.Lys431=
NM_000424.4:c.1293G>A MANE Select	NP_000415.2:p.Lys431=