Canonical Allele Identifier: CA2036492658
Gene: KRT6C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52469596C= , CM000674.2:g.52469596C= GRCh38
NC_000012.11:g.52863380C= , CM000674.1:g.52863380C= GRCh37
NC_000012.10:g.51149647C= NCBI36
NG_012416.1:g.9190G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252250.7:c.1424+74G= MANE Select ENSP00000252250.6:n.1424+74G=
ENST00000252250.6:c.1424+74G= ENSP00000252250.6:n.1424+74G=
NM_173086.4:c.1424+74G= NP_775109.2:n.1424+74G=
NM_173086.5:c.1424+74G= MANE Select NP_775109.2:n.1424+74G=
Search 100 bp 5'
Search 100 bp 3'