Canonical Allele Identifier: CA7523064

Gene: ZSCAN29

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43361124G>A , CM000677.2:g.43361124G>A	GRCh38
NC_000015.9:g.43653322G>A , CM000677.1:g.43653322G>A	GRCh37
NC_000015.8:g.41440614G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001372080.1:c.2508C>T MANE Select	NP_001359009.1:p.His836=
ENST00000684362.1:c.2508C>T MANE Select	ENSP00000507363.1:p.His836=
NM_152455.3:c.2508C>T	NP_689668.3:p.His836=
NM_152455.4:c.2508C>T	NP_689668.3:p.His836=
ENST00000396972.2:c.*1383C>T	ENSP00000380170.2:n.*1383C>T
ENST00000396976.6:c.2508C>T	ENSP00000380174.2:p.His836=
ENST00000562072.5:c.2294C>T	ENSP00000456089.1:n.2294C>T
ENST00000566849.5:c.*1979C>T	ENSP00000457835.1:n.*1979C>T
ENST00000568898.5:c.1338C>T	ENSP00000456883.1:p.His446=
XM_006720401.2:c.2508C>T	XP_006720464.1:p.His836=
XM_011521266.1:c.2508C>T	XP_011519568.1:p.His836=
XM_011521266.2:c.2508C>T	XP_011519568.1:p.His836=
XR_001751103.2:n.2748C>T