Canonical Allele Identifier: CA2036522690

Gene: KRT6A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52492590G= , CM000674.2:g.52492590G=	GRCh38
NC_000012.11:g.52886374G= , CM000674.1:g.52886374G=	GRCh37
NC_000012.10:g.51172641G=	NCBI36
NG_008298.1:g.5808C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330722.7:c.540+59C= MANE Select	ENSP00000369317.3:n.540+59C=
ENST00000330722.6:c.540+59C=	ENSP00000369317.3:n.540+59C=
ENST00000549898.5:n.61+59C=
NM_005554.3:c.540+59C=	NP_005545.1:n.540+59C=
NM_005554.4:c.540+59C= MANE Select	NP_005545.1:n.540+59C=