Canonical Allele Identifier: CA2695238903
Gene: GYS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21559137_21561083del , CM000674.2:g.21559137_21561083del GRCh38
NC_000012.11:g.21712071_21714017del , CM000674.1:g.21712071_21714017del GRCh37
NC_000012.10:g.21603338_21605284del NCBI36
NG_016167.1:g.48768_50714del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.1063-588_1265del
ENST00000647960.1:c.*1065-588_*1267del
ENST00000648372.1:n.990-588_1192del
ENST00000261195.2:c.1063-588_1265del
NM_021957.3:c.1063-588_1265del
XM_005253352.1:c.1063-588_1265del
XM_005253354.2:c.844-588_1046del
XM_006719062.2:c.1063-588_1265del
XM_006719063.2:c.832-588_1034del
NM_021957.4:c.1063-588_1265del
XM_006719063.3:c.832-588_1034del
XM_024448960.1:c.1063-588_1265del