Canonical Allele Identifier: CA480070362

Gene: KRT5

Linked Data

• MyVariant Identifiers: chr12:g.52913649A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519865A>T , CM000674.2:g.52519865A>T	GRCh38
NC_000012.11:g.52913649A>T , CM000674.1:g.52913649A>T	GRCh37
NC_000012.10:g.51199916A>T	NCBI36
NG_008297.1:g.5595T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.432T>A MANE Select	ENSP00000252242.4:p.Thr144=
ENST00000252242.8:c.432T>A	ENSP00000252242.4:p.Thr144=
ENST00000549420.1:c.102T>A	ENSP00000447209.1:p.Thr34=
ENST00000551275.1:c.327T>A	ENSP00000448041.1:p.Thr109=
ENST00000552629.5:n.530T>A
NM_000424.3:c.432T>A	NP_000415.2:p.Thr144=
NM_000424.4:c.432T>A MANE Select	NP_000415.2:p.Thr144=