Canonical Allele Identifier: CA2338594266

Gene: SIX5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45766458G= , CM000681.2:g.45766458G=	GRCh38
NC_000019.9:g.46269716G= , CM000681.1:g.46269716G=	GRCh37
NC_000019.8:g.50961556G=	NCBI36
NG_012745.1:g.7782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.1501C= MANE Select	ENSP00000316842.4:p.Pro501=
ENST00000317578.6:c.1501C=	ENSP00000316842.4:p.Pro501=
ENST00000560160.1:c.587-347C=
ENST00000560168.1:c.*689C=	ENSP00000453189.2:n.*689C=
ENST00000622857.1:c.16-496C=	ENSP00000481365.1:n.16-496C=
NM_175875.4:c.1501C=	NP_787071.2:p.Pro501=
NM_175875.5:c.1501C= MANE Select	NP_787071.3:p.Pro501=