Canonical Allele Identifier: CA406761717
Gene: GYS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974699A>T , CM000681.2:g.48974699A>T GRCh38
NC_000019.9:g.49477956A>T , CM000681.1:g.49477956A>T GRCh37
NC_000019.8:g.54169768A>T NCBI36
NG_012923.1:g.23655T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1343T>A MANE Select ENSP00000317904.3:p.Met448Lys
ENST00000263276.6:c.1151T>A ENSP00000263276.6:p.Met384Lys
ENST00000323798.7:c.1343T>A ENSP00000317904.3:p.Met448Lys
ENST00000472004.5:n.98T>A
ENST00000496048.1:n.250T>A
NM_001161587.1:c.1151T>A NP_001155059.1:p.Met384Lys
NM_002103.4:c.1343T>A NP_002094.2:p.Met448Lys
NR_027763.1:n.1402T>A
NM_002103.5:c.1343T>A MANE Select NP_002094.2:p.Met448Lys
NM_001161587.2:c.1151T>A NP_001155059.1:p.Met384Lys
NR_027763.2:n.1358T>A