Canonical Allele Identifier: CA237234859
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492671_52492673delinsGTT , CM000674.2:g.52492671_52492673delinsGTT GRCh38
NC_000012.11:g.52886455_52886457delinsGTT , CM000674.1:g.52886455_52886457delinsGTT GRCh37
NC_000012.10:g.51172722_51172724delinsGTT NCBI36
NG_008298.1:g.5725_5727delinsAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.516_518delinsAAC MANE Select ENSP00000369317.3:p.Asn172_Lys173delinsLy...
ENST00000330722.6:c.516_518delinsAAC ENSP00000369317.3:p.Asn172_Lys173delinsLy...
ENST00000549898.5:n.37_39delinsAAC
NM_005554.3:c.516_518delinsAAC NP_005545.1:p.Asn172_Lys173delinsLysThr
NM_005554.4:c.516_518delinsAAC MANE Select NP_005545.1:p.Asn172_Lys173delinsLysThr