Canonical Allele Identifier: CA384924140

Gene: KRT5

Linked Data

• MyVariant Identifiers: chr12:g.52910569T>A (hg19) ; chr12:g.52516785T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516785T>A , CM000674.2:g.52516785T>A	GRCh38
NC_000012.11:g.52910569T>A , CM000674.1:g.52910569T>A	GRCh37
NC_000012.10:g.51196836T>A	NCBI36
NG_008297.1:g.8675A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1291A>T MANE Select	ENSP00000252242.4:p.Lys431Ter
ENST00000252242.8:c.1291A>T	ENSP00000252242.4:p.Lys431Ter
ENST00000547890.5:n.669A>T
ENST00000548409.5:c.413A>T
ENST00000549511.5:n.498A>T
ENST00000552629.5:n.1389A>T
NM_000424.3:c.1291A>T	NP_000415.2:p.Lys431Ter
NM_000424.4:c.1291A>T MANE Select	NP_000415.2:p.Lys431Ter