Canonical Allele Identifier: CA479848369

Gene: KRT5

Linked Data

• MyVariant Identifiers: chr12:g.52912912C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519128C>A , CM000674.2:g.52519128C>A	GRCh38
NC_000012.11:g.52912912C>A , CM000674.1:g.52912912C>A	GRCh37
NC_000012.10:g.51199179C>A	NCBI36
NG_008297.1:g.6332G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.588G>T MANE Select	ENSP00000252242.4:p.Leu196=
ENST00000252242.8:c.588G>T	ENSP00000252242.4:p.Leu196=
ENST00000549420.1:c.258G>T	ENSP00000447209.1:p.Leu86=
ENST00000551013.1:n.116G>T
ENST00000552629.5:n.686G>T
NM_000424.3:c.588G>T	NP_000415.2:p.Leu196=
NM_000424.4:c.588G>T MANE Select	NP_000415.2:p.Leu196=