Canonical Allele Identifier: CA2036522624
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492474_52492475delinsTG , CM000674.2:g.52492474_52492475delinsTG GRCh38
NC_000012.11:g.52886258_52886259delinsTG , CM000674.1:g.52886258_52886259delinsTG GRCh37
NC_000012.10:g.51172525_51172526delinsTG NCBI36
NG_008298.1:g.5923_5924delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.540+174_540+175delinsCA MANE Select ENSP00000369317.3:n.540+174_540+175delinsCA
ENST00000330722.6:c.540+174_540+175delinsCA ENSP00000369317.3:n.540+174_540+175delinsCA
ENST00000549898.5:n.61+174_61+175delinsCA
NM_005554.3:c.540+174_540+175delinsCA NP_005545.1:n.540+174_540+175delinsCA
NM_005554.4:c.540+174_540+175delinsCA MANE Select NP_005545.1:n.540+174_540+175delinsCA