Canonical Allele Identifier: CA325966570

Gene: GYG2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2856239C>G , CM000685.2:g.2856239C>G	GRCh38
NC_000023.10:g.2774280C>G , CM000685.1:g.2774280C>G	GRCh37
NC_000023.9:g.2784280C>G	NCBI36
NG_021257.1:g.32418C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001079855.2:c.488-259C>G MANE Select	NP_001073324.1:n.488-259C>G
ENST00000398806.8:c.488-259C>G MANE Select	ENSP00000381786.3:n.488-259C>G
NM_001079855.1:c.488-259C>G	NP_001073324.1:n.488-259C>G
NM_001184702.1:c.488-259C>G	NP_001171631.1:n.488-259C>G
NM_001184702.2:c.488-259C>G	NP_001171631.1:n.488-259C>G
NM_001184703.1:c.581-259C>G	NP_001171632.1:n.581-259C>G
NM_001184703.2:c.581-259C>G	NP_001171632.1:n.581-259C>G
NM_001184704.1:c.23-259C>G	NP_001171633.1:n.23-259C>G
NM_001184704.2:c.23-259C>G	NP_001171633.1:n.23-259C>G
NM_003918.2:c.581-259C>G	NP_003909.2:n.581-259C>G
NM_003918.3:c.581-259C>G	NP_003909.2:n.581-259C>G
ENST00000353656.10:c.581-259C>G	ENSP00000487294.1:n.581-259C>G
ENST00000381157.2:c.36-259C>G
ENST00000381161.5:n.536-259C>G
ENST00000381163.7:c.581-259C>G	ENSP00000370555.3:n.581-259C>G
ENST00000398806.7:c.488-259C>G	ENSP00000381786.3:n.488-259C>G
ENST00000453106.1:n.259-259C>G
ENST00000469234.6:n.441-259C>G
ENST00000639373.1:c.581-259C>G	ENSP00000491962.1:n.581-259C>G
XM_006724521.2:c.581-259C>G	XP_006724584.1:n.581-259C>G
XM_011545600.1:c.488-259C>G	XP_011543902.1:n.488-259C>G
XM_011545600.2:c.488-259C>G	XP_011543902.1:n.488-259C>G
XM_011545601.1:c.575-259C>G	XP_011543903.1:n.575-259C>G
XM_011545602.1:c.23-259C>G	XP_011543904.1:n.23-259C>G
XM_017029927.1:c.581-259C>G	XP_016885416.1:n.581-259C>G
XM_017029928.1:c.581-259C>G	XP_016885417.1:n.581-259C>G
XM_017029929.1:c.581-259C>G	XP_016885418.1:n.581-259C>G
XM_017029930.1:c.488-259C>G	XP_016885419.1:n.488-259C>G
XM_017029931.1:c.488-259C>G	XP_016885420.1:n.488-259C>G