Canonical Allele Identifier: CA405683646

Gene: RYR1

Linked Data

• dbSNP Id: rs1199758037
• gnomAD v3: 19-38510687-T-C
• gnomAD v4: 19-38510687-T-C
• MyVariant Identifiers: chr19:g.39001327T>C (hg19) ; chr19:g.38510687T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38510687T>C , CM000681.2:g.38510687T>C	GRCh38
NC_000019.9:g.39001327T>C , CM000681.1:g.39001327T>C	GRCh37
NC_000019.8:g.43693167T>C	NCBI36
NG_008866.1:g.81988T>C , LRG_766:g.81988T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.9028T>C	ENSP00000471601.2:p.Phe3010Leu
ENST00000359596.8:c.9028T>C MANE Select	ENSP00000352608.2:p.Phe3010Leu
ENST00000355481.8:c.9028T>C	ENSP00000347667.3:p.Phe3010Leu
ENST00000359596.7:c.9028T>C	ENSP00000352608.2:p.Phe3010Leu
ENST00000360985.7:c.9025T>C	ENSP00000354254.4:p.Phe3009Leu
ENST00000594335.5:c.2480T>C
NM_000540.2:c.9028T>C , LRG_766t1:c.9028T>C	NP_000531.2:p.Phe3010Leu
NM_001042723.1:c.9028T>C	NP_001036188.1:p.Phe3010Leu
XM_006723317.1:c.9028T>C	XP_006723380.1:p.Phe3010Leu
XM_006723319.1:c.9028T>C	XP_006723382.1:p.Phe3010Leu
XM_011527204.1:c.9025T>C	XP_011525506.1:p.Phe3009Leu
XM_011527205.1:c.9028T>C	XP_011525507.1:p.Phe3010Leu
XM_006723317.2:c.9028T>C	XP_006723380.1:p.Phe3010Leu
XM_006723319.2:c.9028T>C	XP_006723382.1:p.Phe3010Leu
XM_011527205.2:c.9028T>C	XP_011525507.1:p.Phe3010Leu
XR_001753735.1:n.9111T>C
NM_000540.3:c.9028T>C MANE Select	NP_000531.2:p.Phe3010Leu
NM_001042723.2:c.9028T>C	NP_001036188.1:p.Phe3010Leu