Canonical Allele Identifier: CA2036522692
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1592186383

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492593G>T , CM000674.2:g.52492593G>T GRCh38
NC_000012.11:g.52886377G>T , CM000674.1:g.52886377G>T GRCh37
NC_000012.10:g.51172644G>T NCBI36
NG_008298.1:g.5805C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.540+56C>A MANE Select ENSP00000369317.3:n.540+56C>A
ENST00000330722.6:c.540+56C>A ENSP00000369317.3:n.540+56C>A
ENST00000549898.5:n.61+56C>A
NM_005554.3:c.540+56C>A NP_005545.1:n.540+56C>A
NM_005554.4:c.540+56C>A MANE Select NP_005545.1:n.540+56C>A