Canonical Allele Identifier: CA405674244

Gene: RYR1

Linked Data

• dbSNP Id: rs1245356413
• gnomAD v2: 19-38993598-G-T
• gnomAD v4: 19-38502958-G-T
• MyVariant Identifiers: chr19:g.38993598G>T (hg19) ; chr19:g.38502958G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38502958G>T , CM000681.2:g.38502958G>T	GRCh38
NC_000019.9:g.38993598G>T , CM000681.1:g.38993598G>T	GRCh37
NC_000019.8:g.43685438G>T	NCBI36
NG_008866.1:g.74259G>T , LRG_766:g.74259G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7914G>T	ENSP00000471601.2:p.Lys2638Asn
ENST00000359596.8:c.7914G>T MANE Select	ENSP00000352608.2:p.Lys2638Asn
ENST00000355481.8:c.7914G>T	ENSP00000347667.3:p.Lys2638Asn
ENST00000359596.7:c.7914G>T	ENSP00000352608.2:p.Lys2638Asn
ENST00000360985.7:c.7911G>T	ENSP00000354254.4:p.Lys2637Asn
ENST00000594335.5:c.1366G>T
NM_000540.2:c.7914G>T , LRG_766t1:c.7914G>T	NP_000531.2:p.Lys2638Asn
NM_001042723.1:c.7914G>T	NP_001036188.1:p.Lys2638Asn
XM_006723317.1:c.7914G>T	XP_006723380.1:p.Lys2638Asn
XM_006723319.1:c.7914G>T	XP_006723382.1:p.Lys2638Asn
XM_011527204.1:c.7911G>T	XP_011525506.1:p.Lys2637Asn
XM_011527205.1:c.7914G>T	XP_011525507.1:p.Lys2638Asn
XM_006723317.2:c.7914G>T	XP_006723380.1:p.Lys2638Asn
XM_006723319.2:c.7914G>T	XP_006723382.1:p.Lys2638Asn
XM_011527205.2:c.7914G>T	XP_011525507.1:p.Lys2638Asn
XR_001753735.1:n.7997G>T
NM_000540.3:c.7914G>T MANE Select	NP_000531.2:p.Lys2638Asn
NM_001042723.2:c.7914G>T	NP_001036188.1:p.Lys2638Asn