Canonical Allele Identifier: CA2140896985

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60644892_60644896delinsAAATT , CM000676.2:g.60644892_60644896delinsAAATT	GRCh38
NC_000014.8:g.61111610_61111614delinsAAATT , CM000676.1:g.61111610_61111614delinsAAATT	GRCh37
NC_000014.7:g.60181363_60181367delinsAAATT	NCBI36
NG_008231.1:g.9542_9546delinsAATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645694.3:c.*1387_*1391delinsAATTT MANE Select	ENSP00000494686.1:n.*1387_*1391delinsAATTT
ENST00000247182.6:c.*1387_*1391delinsAATTT	ENSP00000247182.5:n.*1387_*1391delinsAATTT
ENST00000554986.2:c.*1387_*1391delinsAATTT	ENSP00000452700.2:n.*1387_*1391delinsAATTT
NM_005982.3:c.*1387_*1391delinsAATTT	NP_005973.1:n.*1387_*1391delinsAATTT
XM_017021602.2:c.*1661_*1665delinsAATTT	XP_016877091.1:n.*1661_*1665delinsAATTT
NM_005982.4:c.*1387_*1391delinsAATTT MANE Select	NP_005973.1:n.*1387_*1391delinsAATTT