Canonical Allele Identifier: CA2036520387
Gene: KRT6A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488487T= , CM000674.2:g.52488487T= GRCh38
NC_000012.11:g.52882271T= , CM000674.1:g.52882271T= GRCh37
NC_000012.10:g.51168538T= NCBI36
NG_008298.1:g.9911A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1265A= MANE Select ENSP00000369317.3:p.Asp422=
ENST00000330722.6:c.1265A= ENSP00000369317.3:p.Asp422=
NM_005554.3:c.1265A= NP_005545.1:p.Asp422=
NM_005554.4:c.1265A= MANE Select NP_005545.1:p.Asp422=
Search 100 bp 5'
Search 100 bp 3'