Canonical Allele Identifier: CA480069754

Gene: KRT5

Linked Data

• MyVariant Identifiers: chr12:g.52910555C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516771C>A , CM000674.2:g.52516771C>A	GRCh38
NC_000012.11:g.52910555C>A , CM000674.1:g.52910555C>A	GRCh37
NC_000012.10:g.51196822C>A	NCBI36
NG_008297.1:g.8689G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1305G>T MANE Select	ENSP00000252242.4:p.Leu435=
ENST00000252242.8:c.1305G>T	ENSP00000252242.4:p.Leu435=
ENST00000547890.5:n.683G>T
ENST00000548409.5:c.427G>T
ENST00000549511.5:n.512G>T
ENST00000552629.5:n.1403G>T
NM_000424.3:c.1305G>T	NP_000415.2:p.Leu435=
NM_000424.4:c.1305G>T MANE Select	NP_000415.2:p.Leu435=