Canonical Allele Identifier: CA405649700

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39019250G>T (hg19) ; chr19:g.38528610G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38528610G>T , CM000681.2:g.38528610G>T	GRCh38
NC_000019.9:g.39019250G>T , CM000681.1:g.39019250G>T	GRCh37
NC_000019.8:g.43711090G>T	NCBI36
NG_008866.1:g.99911G>T , LRG_766:g.99911G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000599547.6:c.10888G>T	ENSP00000471601.2:n.10888G>T
ENST00000359596.8:c.10949G>T MANE Select	ENSP00000352608.2:p.Cys3650Phe
ENST00000355481.8:c.10934G>T	ENSP00000347667.3:p.Cys3645Phe
ENST00000359596.7:c.10949G>T	ENSP00000352608.2:p.Cys3650Phe
ENST00000360985.7:c.10931G>T	ENSP00000354254.4:p.Cys3644Phe
ENST00000594335.5:c.4336G>T
ENST00000599547.5:c.1756G>T
ENST00000601514.5:c.230G>T	ENSP00000472497.1:p.Cys77Phe
NM_000540.2:c.10949G>T , LRG_766t1:c.10949G>T	NP_000531.2:p.Cys3650Phe
NM_001042723.1:c.10934G>T	NP_001036188.1:p.Cys3645Phe
XM_006723317.1:c.10949G>T	XP_006723380.1:p.Cys3650Phe
XM_006723319.1:c.10934G>T	XP_006723382.1:p.Cys3645Phe
XM_011527204.1:c.10946G>T	XP_011525506.1:p.Cys3649Phe
XM_011527205.1:c.10949G>T	XP_011525507.1:p.Cys3650Phe
XM_006723317.2:c.10949G>T	XP_006723380.1:p.Cys3650Phe
XM_006723319.2:c.10934G>T	XP_006723382.1:p.Cys3645Phe
XM_011527205.2:c.10949G>T	XP_011525507.1:p.Cys3650Phe
NM_000540.3:c.10949G>T MANE Select	NP_000531.2:p.Cys3650Phe
NM_001042723.2:c.10934G>T	NP_001036188.1:p.Cys3645Phe