Canonical Allele Identifier: CA405692407

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39076617A>C (hg19) ; chr19:g.38585977A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38585977A>C , CM000681.2:g.38585977A>C	GRCh38
NC_000019.9:g.39076617A>C , CM000681.1:g.39076617A>C	GRCh37
NC_000019.8:g.43768457A>C	NCBI36
NG_008866.1:g.157278A>C , LRG_766:g.157278A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1779A>C
ENST00000688602.1:c.3176A>C
ENST00000689936.1:c.3148A>C
ENST00000692547.1:n.236A>C
ENST00000359596.8:c.14843A>C MANE Select	ENSP00000352608.2:p.Gln4948Pro
ENST00000355481.8:c.14828A>C	ENSP00000347667.3:p.Gln4943Pro
ENST00000359596.7:c.14843A>C	ENSP00000352608.2:p.Gln4948Pro
ENST00000360985.7:c.14825A>C	ENSP00000354254.4:p.Gln4942Pro
NM_000540.2:c.14843A>C , LRG_766t1:c.14843A>C	NP_000531.2:p.Gln4948Pro
NM_001042723.1:c.14828A>C	NP_001036188.1:p.Gln4943Pro
XM_006723317.1:c.14825A>C	XP_006723380.1:p.Gln4942Pro
XM_006723319.1:c.14810A>C	XP_006723382.1:p.Gln4937Pro
XM_011527204.1:c.14840A>C	XP_011525506.1:p.Gln4947Pro
XM_011527205.1:c.14756A>C	XP_011525507.1:p.Gln4919Pro
XM_006723317.2:c.14825A>C	XP_006723380.1:p.Gln4942Pro
XM_006723319.2:c.14810A>C	XP_006723382.1:p.Gln4937Pro
XM_011527205.2:c.14756A>C	XP_011525507.1:p.Gln4919Pro
NM_000540.3:c.14843A>C MANE Select	NP_000531.2:p.Gln4948Pro
NM_001042723.2:c.14828A>C	NP_001036188.1:p.Gln4943Pro