Canonical Allele Identifier: CA2140896845

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60644735T= , CM000676.2:g.60644735T=	GRCh38
NC_000014.8:g.61111453T= , CM000676.1:g.61111453T=	GRCh37
NC_000014.7:g.60181206T=	NCBI36
NG_008231.1:g.9703A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645694.3:c.*1548A= MANE Select	ENSP00000494686.1:n.*1548A=
ENST00000247182.6:c.*1548A=	ENSP00000247182.5:n.*1548A=
ENST00000554986.2:c.*1548A=	ENSP00000452700.2:n.*1548A=
NM_005982.3:c.*1548A=	NP_005973.1:n.*1548A=
XM_017021602.2:c.*1822A=	XP_016877091.1:n.*1822A=
NM_005982.4:c.*1548A= MANE Select	NP_005973.1:n.*1548A=