Canonical Allele Identifier: CA2618930460
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492571_52492572insGTC , CM000674.2:g.52492571_52492572insGTC GRCh38
NC_000012.11:g.52886355_52886356insGTC , CM000674.1:g.52886355_52886356insGTC GRCh37
NC_000012.10:g.51172622_51172623insGTC NCBI36
NG_008298.1:g.5826_5827insGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+77_540+78insGAC MANE Select ENSP00000369317.3:n.540+77_540+78insGAC
ENST00000330722.6:c.540+77_540+78insGAC ENSP00000369317.3:n.540+77_540+78insGAC
ENST00000549898.5:n.61+77_61+78insGAC
NM_005554.3:c.540+77_540+78insGAC NP_005545.1:n.540+77_540+78insGAC
NM_005554.4:c.540+77_540+78insGAC MANE Select NP_005545.1:n.540+77_540+78insGAC