Canonical Allele Identifier: CA479848529
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913997G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520213G>C , CM000674.2:g.52520213G>C GRCh38
NC_000012.11:g.52913997G>C , CM000674.1:g.52913997G>C GRCh37
NC_000012.10:g.51200264G>C NCBI36
NG_008297.1:g.5247C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.84C>G MANE Select ENSP00000252242.4:p.Ser28=
ENST00000252242.8:c.84C>G ENSP00000252242.4:p.Ser28=
ENST00000546577.1:c.84C>G ENSP00000449651.1:p.Ser28=
ENST00000549420.1:c.43+41C>G ENSP00000447209.1:n.43+41C>G
ENST00000551275.1:c.84C>G ENSP00000448041.1:p.Ser28=
ENST00000552629.5:n.182C>G
NM_000424.3:c.84C>G NP_000415.2:p.Ser28=
NM_000424.4:c.84C>G MANE Select NP_000415.2:p.Ser28=
Search 100 bp 5'
Search 100 bp 3'