Canonical Allele Identifier: CA478869533

Gene: GYS2

Linked Data

• MyVariant Identifiers: chr12:g.21715936A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21563002A>T , CM000674.2:g.21563002A>T	GRCh38
NC_000012.11:g.21715936A>T , CM000674.1:g.21715936A>T	GRCh37
NC_000012.10:g.21607203A>T	NCBI36
NG_016167.1:g.46846T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.978T>A MANE Select	ENSP00000261195.2:p.Leu326=
ENST00000647960.1:c.*980T>A	ENSP00000497202.1:n.*980T>A
ENST00000648372.1:n.905T>A
ENST00000261195.2:c.978T>A	ENSP00000261195.2:p.Leu326=
NM_021957.3:c.978T>A	NP_068776.2:p.Leu326=
XM_005253352.1:c.978T>A	XP_005253409.1:p.Leu326=
XM_005253354.2:c.759T>A	XP_005253411.1:p.Leu253=
XM_006719062.2:c.978T>A	XP_006719125.1:p.Leu326=
XM_006719063.2:c.747T>A	XP_006719126.1:p.Leu249=
NM_021957.4:c.978T>A MANE Select	NP_068776.2:p.Leu326=
XM_006719063.3:c.747T>A	XP_006719126.1:p.Leu249=
XM_017019245.2:c.978T>A	XP_016874734.1:p.Leu326=
XM_024448960.1:c.978T>A	XP_024304728.1:p.Leu326=