Canonical Allele Identifier: CA9090584

Gene: ZBTB7A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4054716dup , CM000681.2:g.4054716dup	GRCh38
NC_000019.9:g.4054714dup , CM000681.1:g.4054714dup	GRCh37
NC_000019.8:g.4005714dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015898.4:c.522dup MANE Select	NP_056982.1:p.Ala175ArgfsTer19
ENST00000322357.9:c.522dup MANE Select	ENSP00000323670.3:p.Ala175ArgfsTer19
NM_001317990.1:c.522dup	NP_001304919.1:p.Ala175ArgfsTer19
NM_001317990.2:c.522dup	NP_001304919.1:p.Ala175ArgfsTer19
NM_015898.2:c.522dup	NP_056982.1:p.Ala175ArgfsTer19
NM_015898.3:c.522dup	NP_056982.1:p.Ala175ArgfsTer19
ENST00000322357.8:c.522dup	ENSP00000323670.3:p.Ala175ArgfsTer19
ENST00000601588.1:c.522dup	ENSP00000471865.1:p.Ala175ArgfsTer19
XM_005259570.3:c.522dup	XP_005259627.2:p.Ala175ArgfsTer19
XM_005259570.5:c.672dup	XP_005259627.3:p.Ala225ArgfsTer19
XM_005259571.3:c.522dup	XP_005259628.1:p.Ala175ArgfsTer19
XM_005259571.4:c.522dup	XP_005259628.1:p.Ala175ArgfsTer19
XM_005259572.2:c.522dup	XP_005259629.1:p.Ala175ArgfsTer19