Canonical Allele Identifier: CA2637772758

Gene: KRT12

Linked Data

• gnomAD v4: 17-40867112-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40867115_40867116del , CM000679.2:g.40867115_40867116del	GRCh38
NC_000017.10:g.39023367_39023368del , CM000679.1:g.39023367_39023368del	GRCh37
NC_000017.9:g.36276893_36276894del	NCBI36
NG_008077.1:g.5097_5098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.73_74del MANE Select	ENSP00000251643.4:p.Ser25CysfsTer?
ENST00000647902.1:c.73_74del	ENSP00000497770.1:p.Ser25CysfsTer?
ENST00000251643.4:c.73_74del	ENSP00000251643.4:p.Ser25CysfsTer?
NM_000223.3:c.73_74del	NP_000214.1:p.Ser25CysfsTer?
XR_934754.1:n.1500+16255_1500+16256del
XR_934754.2:n.2008+16255_2008+16256del
NM_000223.4:c.73_74del MANE Select	NP_000214.1:p.Ser25CysfsTer?