Canonical Allele Identifier: CA507354196

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39002731G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38512091G>C , CM000681.2:g.38512091G>C	GRCh38
NC_000019.9:g.39002731G>C , CM000681.1:g.39002731G>C	GRCh37
NC_000019.8:g.43694571G>C	NCBI36
NG_008866.1:g.83392G>C , LRG_766:g.83392G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000599547.6:c.9173-154G>C	ENSP00000471601.2:n.9173-154G>C
ENST00000359596.8:c.9192G>C MANE Select	ENSP00000352608.2:p.Val3064=
ENST00000355481.8:c.9192G>C	ENSP00000347667.3:p.Val3064=
ENST00000359596.7:c.9192G>C	ENSP00000352608.2:p.Val3064=
ENST00000360985.7:c.9189G>C	ENSP00000354254.4:p.Val3063=
ENST00000594335.5:c.2594G>C
ENST00000599547.5:c.41-154G>C
NM_000540.2:c.9192G>C , LRG_766t1:c.9192G>C	NP_000531.2:p.Val3064=
NM_001042723.1:c.9192G>C	NP_001036188.1:p.Val3064=
XM_006723317.1:c.9192G>C	XP_006723380.1:p.Val3064=
XM_006723319.1:c.9192G>C	XP_006723382.1:p.Val3064=
XM_011527204.1:c.9189G>C	XP_011525506.1:p.Val3063=
XM_011527205.1:c.9192G>C	XP_011525507.1:p.Val3064=
XM_006723317.2:c.9192G>C	XP_006723380.1:p.Val3064=
XM_006723319.2:c.9192G>C	XP_006723382.1:p.Val3064=
XM_011527205.2:c.9192G>C	XP_011525507.1:p.Val3064=
XR_001753735.1:n.9225G>C
NM_000540.3:c.9192G>C MANE Select	NP_000531.2:p.Val3064=
NM_001042723.2:c.9192G>C	NP_001036188.1:p.Val3064=