Canonical Allele Identifier: CA632878111

Gene: RYR1

Linked Data

• dbSNP Id: rs1348655158
• gnomAD v2: 19-39076713-G-A
• gnomAD v4: 19-38586073-G-A
• MyVariant Identifiers: chr19:g.39076713G>A (hg19) ; chr19:g.38586073G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38586073G>A , CM000681.2:g.38586073G>A	GRCh38
NC_000019.9:g.39076713G>A , CM000681.1:g.39076713G>A	GRCh37
NC_000019.8:g.43768553G>A	NCBI36
NG_008866.1:g.157374G>A , LRG_766:g.157374G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1805-18G>A
ENST00000688602.1:c.3202-18G>A
ENST00000689936.1:c.3174-18G>A
ENST00000692547.1:n.262-18G>A
ENST00000359596.8:c.14869-18G>A MANE Select	ENSP00000352608.2:n.14869-18G>A
ENST00000355481.8:c.14854-18G>A	ENSP00000347667.3:n.14854-18G>A
ENST00000359596.7:c.14869-18G>A	ENSP00000352608.2:n.14869-18G>A
ENST00000360985.7:c.14851-18G>A	ENSP00000354254.4:n.14851-18G>A
NM_000540.2:c.14869-18G>A , LRG_766t1:c.14869-18G>A	NP_000531.2:n.14869-18G>A
NM_001042723.1:c.14854-18G>A	NP_001036188.1:n.14854-18G>A
XM_006723317.1:c.14851-18G>A	XP_006723380.1:n.14851-18G>A
XM_006723319.1:c.14836-18G>A	XP_006723382.1:n.14836-18G>A
XM_011527204.1:c.14866-18G>A	XP_011525506.1:n.14866-18G>A
XM_011527205.1:c.14782-18G>A	XP_011525507.1:n.14782-18G>A
XM_006723317.2:c.14851-18G>A	XP_006723380.1:n.14851-18G>A
XM_006723319.2:c.14836-18G>A	XP_006723382.1:n.14836-18G>A
XM_011527205.2:c.14782-18G>A	XP_011525507.1:n.14782-18G>A
NM_000540.3:c.14869-18G>A MANE Select	NP_000531.2:n.14869-18G>A
NM_001042723.2:c.14854-18G>A	NP_001036188.1:n.14854-18G>A