Canonical Allele Identifier: CA2335084665

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565136G= , CM000681.2:g.38565136G=	GRCh38
NC_000019.9:g.39055776G= , CM000681.1:g.39055776G=	GRCh37
NC_000019.8:g.43747616G=	NCBI36
NG_008866.1:g.136437G= , LRG_766:g.136437G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1212G=
ENST00000689936.1:c.1194G=
ENST00000359596.8:c.12802G= MANE Select	ENSP00000352608.2:p.Ala4268=
ENST00000355481.8:c.12787G=	ENSP00000347667.3:p.Ala4263=
ENST00000359596.7:c.12802G=	ENSP00000352608.2:p.Ala4268=
ENST00000360985.7:c.12784G=	ENSP00000354254.4:p.Ala4262=
ENST00000594335.5:c.6171G=
NM_000540.2:c.12802G= , LRG_766t1:c.12802G=	NP_000531.2:p.Ala4268=
NM_001042723.1:c.12787G=	NP_001036188.1:p.Ala4263=
XM_006723317.1:c.12784G=	XP_006723380.1:p.Ala4262=
XM_006723319.1:c.12769G=	XP_006723382.1:p.Ala4257=
XM_011527204.1:c.12799G=	XP_011525506.1:p.Ala4267=
XM_011527205.1:c.12802G=	XP_011525507.1:p.Ala4268=
XM_006723317.2:c.12784G=	XP_006723380.1:p.Ala4262=
XM_006723319.2:c.12769G=	XP_006723382.1:p.Ala4257=
XM_011527205.2:c.12802G=	XP_011525507.1:p.Ala4268=
NM_000540.3:c.12802G= MANE Select	NP_000531.2:p.Ala4268=
NM_001042723.2:c.12787G=	NP_001036188.1:p.Ala4263=