Canonical Allele Identifier: CA384929655

Gene: KRT5

Linked Data

• MyVariant Identifiers: chr12:g.52913722C>A (hg19) ; chr12:g.52519938C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519938C>A , CM000674.2:g.52519938C>A	GRCh38
NC_000012.11:g.52913722C>A , CM000674.1:g.52913722C>A	GRCh37
NC_000012.10:g.51199989C>A	NCBI36
NG_008297.1:g.5522G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.359G>T MANE Select	ENSP00000252242.4:p.Gly120Val
ENST00000252242.8:c.359G>T	ENSP00000252242.4:p.Gly120Val
ENST00000546577.1:c.359G>T	ENSP00000449651.1:p.Gly120Val
ENST00000549420.1:c.44-15G>T	ENSP00000447209.1:n.44-15G>T
ENST00000551275.1:c.254G>T	ENSP00000448041.1:p.Gly85Val
ENST00000552629.5:n.457G>T
NM_000424.3:c.359G>T	NP_000415.2:p.Gly120Val
NM_000424.4:c.359G>T MANE Select	NP_000415.2:p.Gly120Val