Canonical Allele Identifier: CA308679998

Gene: PSG6 PSG7

Linked Data

• dbSNP Id: rs386809477

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42916297_42916299delinsATC , CM000681.2:g.42916297_42916299delinsATC	GRCh38
NC_000019.9:g.43420449_43420451delinsATC , CM000681.1:g.43420449_43420451delinsATC	GRCh37
NC_000019.8:g.48112289_48112291delinsATC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000187910.7:c.253_255delinsGAT (PSG6) MANE Select	ENSP00000187910.3:p.His85Asp
ENST00000187910.6:c.253_255delinsGAT (PSG6)	ENSP00000187910.2:p.His85Asp
ENST00000292125.6:c.253_255delinsGAT (PSG6)	ENSP00000292125.2:p.His85Asp
ENST00000402456.4:n.343_345delinsGAT (PSG6)
ENST00000402603.8:c.253_255delinsGAT (PSG6)	ENSP00000385736.3:p.His85Asp
ENST00000484292.2:n.282+1430_282+1432delinsGAT (PSG6)
ENST00000594375.1:c.64+1430_64+1432delinsGAT (PSG6)	ENSP00000470412.1:n.64+1430_64+1432delinsGAT
ENST00000595062.1:n.100_102delinsGAT (PSG6)
ENST00000601833.1:c.40_42delinsGAT (PSG6)	ENSP00000469423.1:p.His14Asp
ENST00000617049.4:c.989-9123_989-9121delinsGAT (PSG7)	ENSP00000480429.1:n.989-9123_989-9121delinsGAT
NM_001031850.3:c.253_255delinsGAT (PSG6)	NP_001027020.1:p.His85Asp
NM_002782.4:c.253_255delinsGAT (PSG6)	NP_002773.1:p.His85Asp
NM_001031850.4:c.253_255delinsGAT (PSG6) MANE Select	NP_001027020.1:p.His85Asp
NM_002782.5:c.253_255delinsGAT (PSG6)	NP_002773.1:p.His85Asp