Canonical Allele Identifier: CA405662867

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39034462G>T (hg19) ; chr19:g.38543822G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543822G>T , CM000681.2:g.38543822G>T	GRCh38
NC_000019.9:g.39034462G>T , CM000681.1:g.39034462G>T	GRCh37
NC_000019.8:g.43726302G>T	NCBI36
NG_008866.1:g.115123G>T , LRG_766:g.115123G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000688602.1:c.369G>T
ENST00000689936.1:c.351G>T
ENST00000359596.8:c.11959G>T MANE Select	ENSP00000352608.2:p.Ala3987Ser
ENST00000355481.8:c.11944G>T	ENSP00000347667.3:p.Ala3982Ser
ENST00000359596.7:c.11959G>T	ENSP00000352608.2:p.Ala3987Ser
ENST00000360985.7:c.11941G>T	ENSP00000354254.4:p.Ala3981Ser
ENST00000593322.1:c.568G>T
ENST00000594335.5:c.5328G>T
NM_000540.2:c.11959G>T , LRG_766t1:c.11959G>T	NP_000531.2:p.Ala3987Ser
NM_001042723.1:c.11944G>T	NP_001036188.1:p.Ala3982Ser
XM_006723317.1:c.11941G>T	XP_006723380.1:p.Ala3981Ser
XM_006723319.1:c.11926G>T	XP_006723382.1:p.Ala3976Ser
XM_011527204.1:c.11956G>T	XP_011525506.1:p.Ala3986Ser
XM_011527205.1:c.11959G>T	XP_011525507.1:p.Ala3987Ser
XM_006723317.2:c.11941G>T	XP_006723380.1:p.Ala3981Ser
XM_006723319.2:c.11926G>T	XP_006723382.1:p.Ala3976Ser
XM_011527205.2:c.11959G>T	XP_011525507.1:p.Ala3987Ser
NM_000540.3:c.11959G>T MANE Select	NP_000531.2:p.Ala3987Ser
NM_001042723.2:c.11944G>T	NP_001036188.1:p.Ala3982Ser