Canonical Allele Identifier: CA480070330
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913604G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519820G>C , CM000674.2:g.52519820G>C GRCh38
NC_000012.11:g.52913604G>C , CM000674.1:g.52913604G>C GRCh37
NC_000012.10:g.51199871G>C NCBI36
NG_008297.1:g.5640C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.477C>G MANE Select ENSP00000252242.4:p.Pro159=
ENST00000252242.8:c.477C>G ENSP00000252242.4:p.Pro159=
ENST00000549420.1:c.147C>G ENSP00000447209.1:p.Pro49=
ENST00000551275.1:c.372C>G ENSP00000448041.1:p.Pro124=
ENST00000552629.5:n.575C>G
NM_000424.3:c.477C>G NP_000415.2:p.Pro159=
NM_000424.4:c.477C>G MANE Select NP_000415.2:p.Pro159=
Search 100 bp 5'
Search 100 bp 3'