Canonical Allele Identifier: CA2021177004

Gene: GYS2

Linked Data

• dbSNP Id: rs1944223282

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21559337_21559338insG , CM000674.2:g.21559337_21559338insG	GRCh38
NC_000012.11:g.21712271_21712272insG , CM000674.1:g.21712271_21712272insG	GRCh37
NC_000012.10:g.21603538_21603539insG	NCBI36
NG_016167.1:g.50510_50511insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1230-169_1230-168insC MANE Select	ENSP00000261195.2:n.1230-169_1230-168insC
ENST00000647960.1:c.*1232-169_*1232-168insC	ENSP00000497202.1:n.*1232-169_*1232-168insC
ENST00000648372.1:n.1157-169_1157-168insC
ENST00000261195.2:c.1230-169_1230-168insC	ENSP00000261195.2:n.1230-169_1230-168insC
NM_021957.3:c.1230-169_1230-168insC	NP_068776.2:n.1230-169_1230-168insC
XM_005253352.1:c.1230-169_1230-168insC	XP_005253409.1:n.1230-169_1230-168insC
XM_005253354.2:c.1011-169_1011-168insC	XP_005253411.1:n.1011-169_1011-168insC
XM_006719062.2:c.1230-169_1230-168insC	XP_006719125.1:n.1230-169_1230-168insC
XM_006719063.2:c.999-169_999-168insC	XP_006719126.1:n.999-169_999-168insC
NM_021957.4:c.1230-169_1230-168insC MANE Select	NP_068776.2:n.1230-169_1230-168insC
XM_006719063.3:c.999-169_999-168insC	XP_006719126.1:n.999-169_999-168insC
XM_024448960.1:c.1230-169_1230-168insC	XP_024304728.1:n.1230-169_1230-168insC