Canonical Allele Identifier: CA405681471

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39062881C>T (hg19) ; chr19:g.38572241C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572241C>T , CM000681.2:g.38572241C>T	GRCh38
NC_000019.9:g.39062881C>T , CM000681.1:g.39062881C>T	GRCh37
NC_000019.8:g.43754721C>T	NCBI36
NG_008866.1:g.143542C>T , LRG_766:g.143542C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.905C>T
ENST00000688602.1:c.2302C>T
ENST00000689936.1:c.2274C>T
ENST00000359596.8:c.13969C>T MANE Select	ENSP00000352608.2:p.Leu4657Phe
ENST00000355481.8:c.13954C>T	ENSP00000347667.3:p.Leu4652Phe
ENST00000359596.7:c.13969C>T	ENSP00000352608.2:p.Leu4657Phe
ENST00000360985.7:c.13951C>T	ENSP00000354254.4:p.Leu4651Phe
ENST00000593677.1:c.429C>T
NM_000540.2:c.13969C>T , LRG_766t1:c.13969C>T	NP_000531.2:p.Leu4657Phe
NM_001042723.1:c.13954C>T	NP_001036188.1:p.Leu4652Phe
XM_006723317.1:c.13951C>T	XP_006723380.1:p.Leu4651Phe
XM_006723319.1:c.13936C>T	XP_006723382.1:p.Leu4646Phe
XM_011527204.1:c.13966C>T	XP_011525506.1:p.Leu4656Phe
XM_011527205.1:c.13882C>T	XP_011525507.1:p.Leu4628Phe
XM_006723317.2:c.13951C>T	XP_006723380.1:p.Leu4651Phe
XM_006723319.2:c.13936C>T	XP_006723382.1:p.Leu4646Phe
XM_011527205.2:c.13882C>T	XP_011525507.1:p.Leu4628Phe
NM_000540.3:c.13969C>T MANE Select	NP_000531.2:p.Leu4657Phe
NM_001042723.2:c.13954C>T	NP_001036188.1:p.Leu4652Phe