Canonical Allele Identifier: CA2814346189

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38499846dup , CM000681.2:g.38499846dup	GRCh38
NC_000019.9:g.38990486dup , CM000681.1:g.38990486dup	GRCh37
NC_000019.8:g.43682326dup	NCBI36
NG_008866.1:g.71147dup , LRG_766:g.71147dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7214+25dup	ENSP00000471601.2:n.7214+25dup
ENST00000359596.8:c.7214+25dup MANE Select	ENSP00000352608.2:n.7214+25dup
ENST00000355481.8:c.7214+25dup	ENSP00000347667.3:n.7214+25dup
ENST00000359596.7:c.7214+25dup	ENSP00000352608.2:n.7214+25dup
ENST00000360985.7:c.7211+25dup	ENSP00000354254.4:n.7211+25dup
ENST00000594335.5:c.666+25dup
NM_000540.2:c.7214+25dup , LRG_766t1:c.7214+25dup	NP_000531.2:n.7214+25dup
NM_001042723.1:c.7214+25dup	NP_001036188.1:n.7214+25dup
XM_006723317.1:c.7214+25dup	XP_006723380.1:n.7214+25dup
XM_006723319.1:c.7214+25dup	XP_006723382.1:n.7214+25dup
XM_011527204.1:c.7211+25dup	XP_011525506.1:n.7211+25dup
XM_011527205.1:c.7214+25dup	XP_011525507.1:n.7214+25dup
XM_006723317.2:c.7214+25dup	XP_006723380.1:n.7214+25dup
XM_006723319.2:c.7214+25dup	XP_006723382.1:n.7214+25dup
XM_011527205.2:c.7214+25dup	XP_011525507.1:n.7214+25dup
XR_001753735.1:n.7297+25dup
NM_000540.3:c.7214+25dup MANE Select	NP_000531.2:n.7214+25dup
NM_001042723.2:c.7214+25dup	NP_001036188.1:n.7214+25dup