Canonical Allele Identifier: CA406761550
Gene: GYS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49477878T>C (hg19) chr19:g.48974621T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974621T>C , CM000681.2:g.48974621T>C GRCh38
NC_000019.9:g.49477878T>C , CM000681.1:g.49477878T>C GRCh37
NC_000019.8:g.54169690T>C NCBI36
NG_012923.1:g.23733A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1421A>G MANE Select ENSP00000317904.3:p.Lys474Arg
ENST00000263276.6:c.1229A>G ENSP00000263276.6:p.Lys410Arg
ENST00000323798.7:c.1421A>G ENSP00000317904.3:p.Lys474Arg
ENST00000472004.5:n.176A>G
ENST00000496048.1:n.328A>G
NM_001161587.1:c.1229A>G NP_001155059.1:p.Lys410Arg
NM_002103.4:c.1421A>G NP_002094.2:p.Lys474Arg
NR_027763.1:n.1480A>G
NM_002103.5:c.1421A>G MANE Select NP_002094.2:p.Lys474Arg
NM_001161587.2:c.1229A>G NP_001155059.1:p.Lys410Arg
NR_027763.2:n.1436A>G
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