Canonical Allele Identifier: CA384953501
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488395T>C , CM000674.2:g.52488395T>C GRCh38
NC_000012.11:g.52882179T>C , CM000674.1:g.52882179T>C GRCh37
NC_000012.10:g.51168446T>C NCBI36
NG_008298.1:g.10003A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1357A>G MANE Select ENSP00000369317.3:p.Asn453Asp
ENST00000330722.6:c.1357A>G ENSP00000369317.3:p.Asn453Asp
NM_005554.3:c.1357A>G NP_005545.1:p.Asn453Asp
NM_005554.4:c.1357A>G MANE Select NP_005545.1:p.Asn453Asp