Canonical Allele Identifier: CA11758266

Gene: ZGRF1

Linked Data

• dbSNP Id: rs6834538
• gnomAD v2: 4-113544152-T-C
• gnomAD v3: 4-112622996-T-C
• gnomAD v4: 4-112622996-T-C
• MyVariant Identifiers: chr4:g.113544152T>C (hg19) ; chr4:g.112622996T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.112622996T>C , CM000666.2:g.112622996T>C	GRCh38
NC_000004.11:g.113544152T>C , CM000666.1:g.113544152T>C	GRCh37
NC_000004.10:g.113763601T>C	NCBI36
NG_053121.1:g.19000A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000505019.6:c.162+821A>G MANE Select	ENSP00000424737.1:n.162+821A>G
ENST00000264370.9:n.373+821A>G
ENST00000309071.9:c.162+821A>G	ENSP00000309095.5:n.162+821A>G
ENST00000445203.6:c.162+821A>G	ENSP00000390505.3:n.162+821A>G
ENST00000473015.5:c.162+821A>G	ENSP00000426938.1:n.162+821A>G
ENST00000502805.1:c.*233+821A>G	ENSP00000424429.1:n.*233+821A>G
ENST00000503172.5:c.162+821A>G	ENSP00000424995.1:n.162+821A>G
ENST00000505019.5:c.162+821A>G	ENSP00000424737.1:n.162+821A>G
ENST00000512075.1:n.161+821A>G
ENST00000514770.5:c.*276+821A>G	ENSP00000424946.1:n.*276+821A>G
NM_018392.4:c.162+821A>G	NP_060862.3:n.162+821A>G
XM_005263115.2:c.162+821A>G	XP_005263172.1:n.162+821A>G
XM_011532091.1:c.162+821A>G	XP_011530393.1:n.162+821A>G
XM_011532092.1:c.103-2806A>G	XP_011530394.1:n.103-2806A>G
XM_011532093.1:c.162+821A>G	XP_011530395.1:n.162+821A>G
XM_011532094.1:c.162+821A>G	XP_011530396.1:n.162+821A>G
XM_011532095.1:c.162+821A>G	XP_011530397.1:n.162+821A>G
XM_011532096.1:c.162+821A>G	XP_011530398.1:n.162+821A>G
XR_938763.1:n.373+821A>G
XR_938764.1:n.373+821A>G
NM_001350397.1:c.162+821A>G	NP_001337326.1:n.162+821A>G
XM_005263115.4:c.162+821A>G	XP_005263172.1:n.162+821A>G
XM_011532091.2:c.162+821A>G	XP_011530393.1:n.162+821A>G
XM_011532092.2:c.103-2806A>G	XP_011530394.1:n.103-2806A>G
XM_011532094.2:c.162+821A>G	XP_011530396.1:n.162+821A>G
XM_011532096.2:c.162+821A>G	XP_011530398.1:n.162+821A>G
XM_017008369.2:c.103-2806A>G	XP_016863858.1:n.103-2806A>G
XM_017008370.1:c.162+821A>G	XP_016863859.1:n.162+821A>G
XM_017008371.1:c.103-2806A>G	XP_016863860.1:n.103-2806A>G
XM_017008372.1:c.-2714+821A>G	XP_016863861.1:n.-2714+821A>G
XM_017008373.1:c.-2713-2806A>G	XP_016863862.1:n.-2713-2806A>G
XR_001741282.1:n.373+821A>G
NM_001350397.2:c.162+821A>G	NP_001337326.1:n.162+821A>G
NM_018392.5:c.162+821A>G MANE Select	NP_060862.3:n.162+821A>G