Canonical Allele Identifier: CA405694073

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39077985G>T (hg19) ; chr19:g.38587345G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38587345G>T , CM000681.2:g.38587345G>T	GRCh38
NC_000019.9:g.39077985G>T , CM000681.1:g.39077985G>T	GRCh37
NC_000019.8:g.43769825G>T	NCBI36
NG_008866.1:g.158646G>T , LRG_766:g.158646G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1957+769G>T
ENST00000688602.1:c.3375G>T
ENST00000689936.1:c.3347G>T
ENST00000692547.1:n.435G>T
ENST00000359596.8:c.15042G>T MANE Select	ENSP00000352608.2:p.Met5014Ile
ENST00000355481.8:c.15027G>T	ENSP00000347667.3:p.Met5009Ile
ENST00000359596.7:c.15042G>T	ENSP00000352608.2:p.Met5014Ile
ENST00000360985.7:c.15024G>T	ENSP00000354254.4:p.Met5008Ile
NM_000540.2:c.15042G>T , LRG_766t1:c.15042G>T	NP_000531.2:p.Met5014Ile
NM_001042723.1:c.15027G>T	NP_001036188.1:p.Met5009Ile
XM_006723317.1:c.15024G>T	XP_006723380.1:p.Met5008Ile
XM_006723319.1:c.15009G>T	XP_006723382.1:p.Met5003Ile
XM_011527204.1:c.15039G>T	XP_011525506.1:p.Met5013Ile
XM_011527205.1:c.14955G>T	XP_011525507.1:p.Met4985Ile
XM_006723317.2:c.15024G>T	XP_006723380.1:p.Met5008Ile
XM_006723319.2:c.15009G>T	XP_006723382.1:p.Met5003Ile
XM_011527205.2:c.14955G>T	XP_011525507.1:p.Met4985Ile
NM_000540.3:c.15042G>T MANE Select	NP_000531.2:p.Met5014Ile
NM_001042723.2:c.15027G>T	NP_001036188.1:p.Met5009Ile