Canonical Allele Identifier: CA2741038648

Gene: ZNF510

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96776745A>G , CM000671.2:g.96776745A>G	GRCh38
NC_000009.11:g.99539027A>G , CM000671.1:g.99539027A>G	GRCh37
NC_000009.10:g.98578848A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223428.9:c.-176-500T>C MANE Select	ENSP00000223428.4:n.-176-500T>C
ENST00000223428.8:c.-176-500T>C	ENSP00000223428.4:n.-176-500T>C
ENST00000374641.3:c.-176-500T>C	ENSP00000363772.3:n.-176-500T>C
ENST00000375231.5:c.-176-500T>C	ENSP00000364379.1:n.-176-500T>C
NM_001314059.1:c.-176-500T>C	NP_001300988.1:n.-176-500T>C
NM_001314060.1:c.-303-500T>C	NP_001300989.1:n.-303-500T>C
NM_014930.1:c.-176-500T>C	NP_055745.1:n.-176-500T>C
NM_014930.2:c.-176-500T>C	NP_055745.1:n.-176-500T>C
XM_005251807.2:c.-176-500T>C	XP_005251864.1:n.-176-500T>C
XM_005251808.2:c.-176-500T>C	XP_005251865.1:n.-176-500T>C
XM_005251809.2:c.-303-500T>C	XP_005251866.1:n.-303-500T>C
XM_011518393.2:c.-387-500T>C	XP_011516695.1:n.-387-500T>C
XM_017014483.1:c.-176-500T>C	XP_016869972.1:n.-176-500T>C
NM_001314059.2:c.-176-500T>C	NP_001300988.1:n.-176-500T>C
NM_001314060.2:c.-303-500T>C	NP_001300989.1:n.-303-500T>C
NM_014930.3:c.-176-500T>C MANE Select	NP_055745.1:n.-176-500T>C