Canonical Allele Identifier: CA2843262394

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38499056A>T , CM000681.2:g.38499056A>T	GRCh38
NC_000019.9:g.38989696A>T , CM000681.1:g.38989696A>T	GRCh37
NC_000019.8:g.43681536A>T	NCBI36
NG_008866.1:g.70357A>T , LRG_766:g.70357A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.6892-52A>T	ENSP00000471601.2:n.6892-52A>T
ENST00000359596.8:c.6892-52A>T MANE Select	ENSP00000352608.2:n.6892-52A>T
ENST00000355481.8:c.6892-52A>T	ENSP00000347667.3:n.6892-52A>T
ENST00000359596.7:c.6892-52A>T	ENSP00000352608.2:n.6892-52A>T
ENST00000360985.7:c.6889-52A>T	ENSP00000354254.4:n.6889-52A>T
ENST00000594335.5:c.344-52A>T
NM_000540.2:c.6892-52A>T , LRG_766t1:c.6892-52A>T	NP_000531.2:n.6892-52A>T
NM_001042723.1:c.6892-52A>T	NP_001036188.1:n.6892-52A>T
XM_006723317.1:c.6892-52A>T	XP_006723380.1:n.6892-52A>T
XM_006723319.1:c.6892-52A>T	XP_006723382.1:n.6892-52A>T
XM_011527204.1:c.6889-52A>T	XP_011525506.1:n.6889-52A>T
XM_011527205.1:c.6892-52A>T	XP_011525507.1:n.6892-52A>T
XM_006723317.2:c.6892-52A>T	XP_006723380.1:n.6892-52A>T
XM_006723319.2:c.6892-52A>T	XP_006723382.1:n.6892-52A>T
XM_011527205.2:c.6892-52A>T	XP_011525507.1:n.6892-52A>T
XR_001753735.1:n.6975-52A>T
NM_000540.3:c.6892-52A>T MANE Select	NP_000531.2:n.6892-52A>T
NM_001042723.2:c.6892-52A>T	NP_001036188.1:n.6892-52A>T