Canonical Allele Identifier: CA1977850378

Gene: GANAB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62626633G= , CM000673.2:g.62626633G=	GRCh38
NC_000011.9:g.62394105G= , CM000673.1:g.62394105G=	GRCh37
NC_000011.8:g.62150681G=	NCBI36
NG_031863.1:g.543C=
NG_053018.1:g.25094C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356638.8:c.2449C= MANE Select	ENSP00000349053.3:p.Arg817=
ENST00000648273.1:c.2158C=	ENSP00000497655.1:p.Arg720=
ENST00000346178.8:c.2515C=	ENSP00000340466.4:p.Arg839=
ENST00000356638.7:c.2449C=	ENSP00000349053.3:p.Arg817=
ENST00000528503.1:n.138C=
ENST00000531563.1:n.304C=
ENST00000532402.5:c.*2181C=	ENSP00000432181.1:n.*2181C=
ENST00000534779.5:c.2173C=	ENSP00000435306.1:p.Arg725=
ENST00000540933.5:c.2158C=	ENSP00000442962.1:p.Arg720=
NM_001278192.1:c.2173C=	NP_001265121.1:p.Arg725=
NM_001278193.1:c.2107C=	NP_001265122.1:p.Arg703=
NM_001278194.1:c.2158C=	NP_001265123.1:p.Arg720=
NM_198334.2:c.2449C=	NP_938148.1:p.Arg817=
NM_198335.3:c.2515C=	NP_938149.2:p.Arg839=
NM_001329222.1:c.2158C=	NP_001316151.1:p.Arg720=
NM_001329223.1:c.2158C=	NP_001316152.1:p.Arg720=
NM_001329224.1:c.1726C=	NP_001316153.1:p.Arg576=
NM_001329225.1:c.1726C=	NP_001316154.1:p.Arg576=
XM_017017412.1:c.2158C=	XP_016872901.1:p.Arg720=
NM_198334.3:c.2449C= MANE Select	NP_938148.1:p.Arg817=
NM_001278192.2:c.2173C=	NP_001265121.1:p.Arg725=
NM_001278193.2:c.2107C=	NP_001265122.1:p.Arg703=
NM_001329223.2:c.2158C=	NP_001316152.1:p.Arg720=
NM_001329225.2:c.1726C=	NP_001316154.1:p.Arg576=
NM_198335.4:c.2515C=	NP_938149.2:p.Arg839=
NM_001278194.2:c.2158C=	NP_001265123.1:p.Arg720=
NM_001329222.2:c.2158C=	NP_001316151.1:p.Arg720=
NM_001329224.2:c.1726C=	NP_001316153.1:p.Arg576=