Canonical Allele Identifier: CA2335092493

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580456G= , CM000681.2:g.38580456G=	GRCh38
NC_000019.9:g.39071096G= , CM000681.1:g.39071096G=	GRCh37
NC_000019.8:g.43762936G=	NCBI36
NG_008866.1:g.151757G= , LRG_766:g.151757G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1534G=
ENST00000688602.1:c.2931G=
ENST00000689936.1:c.2903G=
ENST00000359596.8:c.14598G= MANE Select	ENSP00000352608.2:p.Lys4866=
ENST00000355481.8:c.14583G=	ENSP00000347667.3:p.Lys4861=
ENST00000359596.7:c.14598G=	ENSP00000352608.2:p.Lys4866=
ENST00000360985.7:c.14580G=	ENSP00000354254.4:p.Lys4860=
NM_000540.2:c.14598G= , LRG_766t1:c.14598G=	NP_000531.2:p.Lys4866=
NM_001042723.1:c.14583G=	NP_001036188.1:p.Lys4861=
XM_006723317.1:c.14580G=	XP_006723380.1:p.Lys4860=
XM_006723319.1:c.14565G=	XP_006723382.1:p.Lys4855=
XM_011527204.1:c.14595G=	XP_011525506.1:p.Lys4865=
XM_011527205.1:c.14511G=	XP_011525507.1:p.Lys4837=
XM_006723317.2:c.14580G=	XP_006723380.1:p.Lys4860=
XM_006723319.2:c.14565G=	XP_006723382.1:p.Lys4855=
XM_011527205.2:c.14511G=	XP_011525507.1:p.Lys4837=
NM_000540.3:c.14598G= MANE Select	NP_000531.2:p.Lys4866=
NM_001042723.2:c.14583G=	NP_001036188.1:p.Lys4861=