Canonical Allele Identifier: CA384953521
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488400A>C , CM000674.2:g.52488400A>C GRCh38
NC_000012.11:g.52882184A>C , CM000674.1:g.52882184A>C GRCh37
NC_000012.10:g.51168451A>C NCBI36
NG_008298.1:g.9998T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1352T>G MANE Select ENSP00000369317.3:p.Leu451Arg
ENST00000330722.6:c.1352T>G ENSP00000369317.3:p.Leu451Arg
NM_005554.3:c.1352T>G NP_005545.1:p.Leu451Arg
NM_005554.4:c.1352T>G MANE Select NP_005545.1:p.Leu451Arg