Canonical Allele Identifier: CA405687636

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071037G>A (hg19) ; chr19:g.38580397G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580397G>A , CM000681.2:g.38580397G>A	GRCh38
NC_000019.9:g.39071037G>A , CM000681.1:g.39071037G>A	GRCh37
NC_000019.8:g.43762877G>A	NCBI36
NG_008866.1:g.151698G>A , LRG_766:g.151698G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1475G>A
ENST00000688602.1:c.2872G>A
ENST00000689936.1:c.2844G>A
ENST00000359596.8:c.14539G>A MANE Select	ENSP00000352608.2:p.Val4847Met
ENST00000355481.8:c.14524G>A	ENSP00000347667.3:p.Val4842Met
ENST00000359596.7:c.14539G>A	ENSP00000352608.2:p.Val4847Met
ENST00000360985.7:c.14521G>A	ENSP00000354254.4:p.Val4841Met
NM_000540.2:c.14539G>A , LRG_766t1:c.14539G>A	NP_000531.2:p.Val4847Met
NM_001042723.1:c.14524G>A	NP_001036188.1:p.Val4842Met
XM_006723317.1:c.14521G>A	XP_006723380.1:p.Val4841Met
XM_006723319.1:c.14506G>A	XP_006723382.1:p.Val4836Met
XM_011527204.1:c.14536G>A	XP_011525506.1:p.Val4846Met
XM_011527205.1:c.14452G>A	XP_011525507.1:p.Val4818Met
XM_006723317.2:c.14521G>A	XP_006723380.1:p.Val4841Met
XM_006723319.2:c.14506G>A	XP_006723382.1:p.Val4836Met
XM_011527205.2:c.14452G>A	XP_011525507.1:p.Val4818Met
NM_000540.3:c.14539G>A MANE Select	NP_000531.2:p.Val4847Met
NM_001042723.2:c.14524G>A	NP_001036188.1:p.Val4842Met