Canonical Allele Identifier: CA405681405

Gene: RYR1

Linked Data

• gnomAD v4: 19-38572233-T-C
• MyVariant Identifiers: chr19:g.39062873T>C (hg19) ; chr19:g.38572233T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572233T>C , CM000681.2:g.38572233T>C	GRCh38
NC_000019.9:g.39062873T>C , CM000681.1:g.39062873T>C	GRCh37
NC_000019.8:g.43754713T>C	NCBI36
NG_008866.1:g.143534T>C , LRG_766:g.143534T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.897T>C
ENST00000688602.1:c.2294T>C
ENST00000689936.1:c.2266T>C
ENST00000359596.8:c.13961T>C MANE Select	ENSP00000352608.2:p.Val4654Ala
ENST00000355481.8:c.13946T>C	ENSP00000347667.3:p.Val4649Ala
ENST00000359596.7:c.13961T>C	ENSP00000352608.2:p.Val4654Ala
ENST00000360985.7:c.13943T>C	ENSP00000354254.4:p.Val4648Ala
ENST00000593677.1:c.421T>C
NM_000540.2:c.13961T>C , LRG_766t1:c.13961T>C	NP_000531.2:p.Val4654Ala
NM_001042723.1:c.13946T>C	NP_001036188.1:p.Val4649Ala
XM_006723317.1:c.13943T>C	XP_006723380.1:p.Val4648Ala
XM_006723319.1:c.13928T>C	XP_006723382.1:p.Val4643Ala
XM_011527204.1:c.13958T>C	XP_011525506.1:p.Val4653Ala
XM_011527205.1:c.13874T>C	XP_011525507.1:p.Val4625Ala
XM_006723317.2:c.13943T>C	XP_006723380.1:p.Val4648Ala
XM_006723319.2:c.13928T>C	XP_006723382.1:p.Val4643Ala
XM_011527205.2:c.13874T>C	XP_011525507.1:p.Val4625Ala
NM_000540.3:c.13961T>C MANE Select	NP_000531.2:p.Val4654Ala
NM_001042723.2:c.13946T>C	NP_001036188.1:p.Val4649Ala