Canonical Allele Identifier: CA405681564

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39062902T>A (hg19) ; chr19:g.38572262T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572262T>A , CM000681.2:g.38572262T>A	GRCh38
NC_000019.9:g.39062902T>A , CM000681.1:g.39062902T>A	GRCh37
NC_000019.8:g.43754742T>A	NCBI36
NG_008866.1:g.143563T>A , LRG_766:g.143563T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.926T>A
ENST00000688602.1:c.2323T>A
ENST00000689936.1:c.2295T>A
ENST00000359596.8:c.13990T>A MANE Select	ENSP00000352608.2:p.Cys4664Ser
ENST00000355481.8:c.13975T>A	ENSP00000347667.3:p.Cys4659Ser
ENST00000359596.7:c.13990T>A	ENSP00000352608.2:p.Cys4664Ser
ENST00000360985.7:c.13972T>A	ENSP00000354254.4:p.Cys4658Ser
NM_000540.2:c.13990T>A , LRG_766t1:c.13990T>A	NP_000531.2:p.Cys4664Ser
NM_001042723.1:c.13975T>A	NP_001036188.1:p.Cys4659Ser
XM_006723317.1:c.13972T>A	XP_006723380.1:p.Cys4658Ser
XM_006723319.1:c.13957T>A	XP_006723382.1:p.Cys4653Ser
XM_011527204.1:c.13987T>A	XP_011525506.1:p.Cys4663Ser
XM_011527205.1:c.13903T>A	XP_011525507.1:p.Cys4635Ser
XM_006723317.2:c.13972T>A	XP_006723380.1:p.Cys4658Ser
XM_006723319.2:c.13957T>A	XP_006723382.1:p.Cys4653Ser
XM_011527205.2:c.13903T>A	XP_011525507.1:p.Cys4635Ser
NM_000540.3:c.13990T>A MANE Select	NP_000531.2:p.Cys4664Ser
NM_001042723.2:c.13975T>A	NP_001036188.1:p.Cys4659Ser