Canonical Allele Identifier: CA500187421
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023275del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867027del , CM000679.2:g.40867027del GRCh38
NC_000017.10:g.39023279del , CM000679.1:g.39023279del GRCh37
NC_000017.9:g.36276805del NCBI36
NG_008077.1:g.5188del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.164del MANE Select ENSP00000251643.4:p.Gly55GlufsTer?
ENST00000647902.1:c.164del ENSP00000497770.1:p.Gly55GlufsTer20
ENST00000251643.4:c.164del ENSP00000251643.4:p.Gly55GlufsTer?
NM_000223.3:c.164del NP_000214.1:p.Gly55GlufsTer?
XR_934754.1:n.1500+16167del
XR_934754.2:n.2008+16167del
NM_000223.4:c.164del MANE Select NP_000214.1:p.Gly55GlufsTer?