Canonical Allele Identifier: CA2335344635

Gene: ACP7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39090097A>T , CM000681.2:g.39090097A>T	GRCh38
NC_000019.9:g.39580737A>T , CM000681.1:g.39580737A>T	GRCh37
NC_000019.8:g.44272577A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331256.10:c.121+4707A>T MANE Select	ENSP00000327557.4:n.121+4707A>T
ENST00000331256.9:c.121+4707A>T	ENSP00000327557.4:n.121+4707A>T
ENST00000594229.1:c.121+4707A>T	ENSP00000470989.1:n.121+4707A>T
ENST00000601575.5:c.121+4707A>T	ENSP00000469048.1:n.121+4707A>T
NM_001004318.2:c.121+4707A>T	NP_001004318.2:n.121+4707A>T
XM_011526966.1:c.121+4707A>T	XP_011525268.1:n.121+4707A>T
XM_011526967.1:c.121+4707A>T	XP_011525269.1:n.121+4707A>T
XM_011526968.1:c.121+4707A>T	XP_011525270.1:n.121+4707A>T
XM_011526969.1:c.121+4707A>T	XP_011525271.1:n.121+4707A>T
NM_001363687.1:c.121+4707A>T	NP_001350616.1:n.121+4707A>T
XM_011526966.3:c.121+4707A>T	XP_011525268.1:n.121+4707A>T
XM_011526967.3:c.121+4707A>T	XP_011525269.1:n.121+4707A>T
XM_011526969.2:c.121+4707A>T	XP_011525271.1:n.121+4707A>T
XM_017026807.2:c.121+4707A>T	XP_016882296.1:n.121+4707A>T
XM_017026808.2:c.-416+4707A>T	XP_016882297.1:n.-416+4707A>T
XR_001753684.2:n.395+4707A>T
NM_001004318.3:c.121+4707A>T MANE Select	NP_001004318.2:n.121+4707A>T
NM_001363687.2:c.121+4707A>T	NP_001350616.1:n.121+4707A>T