Canonical Allele Identifier: CA2036520246
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488241_52488242delinsAT , CM000674.2:g.52488241_52488242delinsAT GRCh38
NC_000012.11:g.52882025_52882026delinsAT , CM000674.1:g.52882025_52882026delinsAT GRCh37
NC_000012.10:g.51168292_51168293delinsAT NCBI36
NG_008298.1:g.10156_10157delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1424+86_1424+87delinsAT MANE Select ENSP00000369317.3:n.1424+86_1424+87delinsAT
ENST00000330722.6:c.1424+86_1424+87delinsAT ENSP00000369317.3:n.1424+86_1424+87delinsAT
NM_005554.3:c.1424+86_1424+87delinsAT NP_005545.1:n.1424+86_1424+87delinsAT
NM_005554.4:c.1424+86_1424+87delinsAT MANE Select NP_005545.1:n.1424+86_1424+87delinsAT