Canonical Allele Identifier: CA405686979

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39070664G>C (hg19) ; chr19:g.38580024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580024G>C , CM000681.2:g.38580024G>C	GRCh38
NC_000019.9:g.39070664G>C , CM000681.1:g.39070664G>C	GRCh37
NC_000019.8:g.43762504G>C	NCBI36
NG_008866.1:g.151325G>C , LRG_766:g.151325G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1343G>C
ENST00000688602.1:c.2740G>C
ENST00000689936.1:c.2712G>C
ENST00000359596.8:c.14407G>C MANE Select	ENSP00000352608.2:p.Gly4803Arg
ENST00000355481.8:c.14392G>C	ENSP00000347667.3:p.Gly4798Arg
ENST00000359596.7:c.14407G>C	ENSP00000352608.2:p.Gly4803Arg
ENST00000360985.7:c.14389G>C	ENSP00000354254.4:p.Gly4797Arg
NM_000540.2:c.14407G>C , LRG_766t1:c.14407G>C	NP_000531.2:p.Gly4803Arg
NM_001042723.1:c.14392G>C	NP_001036188.1:p.Gly4798Arg
XM_006723317.1:c.14389G>C	XP_006723380.1:p.Gly4797Arg
XM_006723319.1:c.14374G>C	XP_006723382.1:p.Gly4792Arg
XM_011527204.1:c.14404G>C	XP_011525506.1:p.Gly4802Arg
XM_011527205.1:c.14320G>C	XP_011525507.1:p.Gly4774Arg
XM_006723317.2:c.14389G>C	XP_006723380.1:p.Gly4797Arg
XM_006723319.2:c.14374G>C	XP_006723382.1:p.Gly4792Arg
XM_011527205.2:c.14320G>C	XP_011525507.1:p.Gly4774Arg
NM_000540.3:c.14407G>C MANE Select	NP_000531.2:p.Gly4803Arg
NM_001042723.2:c.14392G>C	NP_001036188.1:p.Gly4798Arg