Canonical Allele Identifier: CA507245189

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063933G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573293G>C , CM000681.2:g.38573293G>C	GRCh38
NC_000019.9:g.39063933G>C , CM000681.1:g.39063933G>C	GRCh37
NC_000019.8:g.43755773G>C	NCBI36
NG_008866.1:g.144594G>C , LRG_766:g.144594G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1051G>C
ENST00000688602.1:c.2448G>C
ENST00000689936.1:c.2420G>C
ENST00000359596.8:c.14115G>C MANE Select	ENSP00000352608.2:p.Leu4705=
ENST00000355481.8:c.14100G>C	ENSP00000347667.3:p.Leu4700=
ENST00000359596.7:c.14115G>C	ENSP00000352608.2:p.Leu4705=
ENST00000360985.7:c.14097G>C	ENSP00000354254.4:p.Leu4699=
NM_000540.2:c.14115G>C , LRG_766t1:c.14115G>C	NP_000531.2:p.Leu4705=
NM_001042723.1:c.14100G>C	NP_001036188.1:p.Leu4700=
XM_006723317.1:c.14097G>C	XP_006723380.1:p.Leu4699=
XM_006723319.1:c.14082G>C	XP_006723382.1:p.Leu4694=
XM_011527204.1:c.14112G>C	XP_011525506.1:p.Leu4704=
XM_011527205.1:c.14028G>C	XP_011525507.1:p.Leu4676=
XM_006723317.2:c.14097G>C	XP_006723380.1:p.Leu4699=
XM_006723319.2:c.14082G>C	XP_006723382.1:p.Leu4694=
XM_011527205.2:c.14028G>C	XP_011525507.1:p.Leu4676=
NM_000540.3:c.14115G>C MANE Select	NP_000531.2:p.Leu4705=
NM_001042723.2:c.14100G>C	NP_001036188.1:p.Leu4700=