Canonical Allele Identifier: CA2036520265
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488275_52488276delinsAG , CM000674.2:g.52488275_52488276delinsAG GRCh38
NC_000012.11:g.52882059_52882060delinsAG , CM000674.1:g.52882059_52882060delinsAG GRCh37
NC_000012.10:g.51168326_51168327delinsAG NCBI36
NG_008298.1:g.10122_10123delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1424+52_1424+53delinsCT MANE Select ENSP00000369317.3:n.1424+52_1424+53delinsCT
ENST00000330722.6:c.1424+52_1424+53delinsCT ENSP00000369317.3:n.1424+52_1424+53delinsCT
NM_005554.3:c.1424+52_1424+53delinsCT NP_005545.1:n.1424+52_1424+53delinsCT
NM_005554.4:c.1424+52_1424+53delinsCT MANE Select NP_005545.1:n.1424+52_1424+53delinsCT