Canonical Allele Identifier: CA2036520131
Gene: KRT6A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488037G= , CM000674.2:g.52488037G= GRCh38
NC_000012.11:g.52881821G= , CM000674.1:g.52881821G= GRCh37
NC_000012.10:g.51168088G= NCBI36
NG_008298.1:g.10361C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1459+32C= MANE Select ENSP00000369317.3:n.1459+32C=
ENST00000330722.6:c.1459+32C= ENSP00000369317.3:n.1459+32C=
NM_005554.3:c.1459+32C= NP_005545.1:n.1459+32C=
NM_005554.4:c.1459+32C= MANE Select NP_005545.1:n.1459+32C=
Search 100 bp 5'
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