Canonical Allele Identifier: CA1866197878

Gene: ZNF510

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96777150A= , CM000671.2:g.96777150A=	GRCh38
NC_000009.11:g.99539432A= , CM000671.1:g.99539432A=	GRCh37
NC_000009.10:g.98579253A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223428.9:c.-177+884T= MANE Select	ENSP00000223428.4:n.-177+884T=
ENST00000223428.8:c.-177+884T=	ENSP00000223428.4:n.-177+884T=
ENST00000374641.3:c.-177+884T=	ENSP00000363772.3:n.-177+884T=
ENST00000375231.5:c.-177+432T=	ENSP00000364379.1:n.-177+432T=
NM_001314059.1:c.-177+432T=	NP_001300988.1:n.-177+432T=
NM_001314060.1:c.-304+884T=	NP_001300989.1:n.-304+884T=
NM_014930.1:c.-177+884T=	NP_055745.1:n.-177+884T=
NM_014930.2:c.-177+884T=	NP_055745.1:n.-177+884T=
XM_005251807.2:c.-177+432T=	XP_005251864.1:n.-177+432T=
XM_005251808.2:c.-177+884T=	XP_005251865.1:n.-177+884T=
XM_005251809.2:c.-304+884T=	XP_005251866.1:n.-304+884T=
XM_011518393.2:c.-388+884T=	XP_011516695.1:n.-388+884T=
XM_017014483.1:c.-177+432T=	XP_016869972.1:n.-177+432T=
NM_001314059.2:c.-177+432T=	NP_001300988.1:n.-177+432T=
NM_001314060.2:c.-304+884T=	NP_001300989.1:n.-304+884T=
NM_014930.3:c.-177+884T= MANE Select	NP_055745.1:n.-177+884T=