Canonical Allele Identifier: CA384924130

Gene: KRT5

Linked Data

• MyVariant Identifiers: chr12:g.52910568T>A (hg19) ; chr12:g.52516784T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516784T>A , CM000674.2:g.52516784T>A	GRCh38
NC_000012.11:g.52910568T>A , CM000674.1:g.52910568T>A	GRCh37
NC_000012.10:g.51196835T>A	NCBI36
NG_008297.1:g.8676A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1292A>T MANE Select	ENSP00000252242.4:p.Lys431Met
ENST00000252242.8:c.1292A>T	ENSP00000252242.4:p.Lys431Met
ENST00000547890.5:n.670A>T
ENST00000548409.5:c.414A>T
ENST00000549511.5:n.499A>T
ENST00000552629.5:n.1390A>T
NM_000424.3:c.1292A>T	NP_000415.2:p.Lys431Met
NM_000424.4:c.1292A>T MANE Select	NP_000415.2:p.Lys431Met