Canonical Allele Identifier: CA2036522646
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492505_52492506delinsTG , CM000674.2:g.52492505_52492506delinsTG GRCh38
NC_000012.11:g.52886289_52886290delinsTG , CM000674.1:g.52886289_52886290delinsTG GRCh37
NC_000012.10:g.51172556_51172557delinsTG NCBI36
NG_008298.1:g.5892_5893delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.540+143_540+144delinsCA MANE Select ENSP00000369317.3:n.540+143_540+144delinsCA
ENST00000330722.6:c.540+143_540+144delinsCA ENSP00000369317.3:n.540+143_540+144delinsCA
ENST00000549898.5:n.61+143_61+144delinsCA
NM_005554.3:c.540+143_540+144delinsCA NP_005545.1:n.540+143_540+144delinsCA
NM_005554.4:c.540+143_540+144delinsCA MANE Select NP_005545.1:n.540+143_540+144delinsCA