Canonical Allele Identifier: CA507356233

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39062880T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572240T>C , CM000681.2:g.38572240T>C	GRCh38
NC_000019.9:g.39062880T>C , CM000681.1:g.39062880T>C	GRCh37
NC_000019.8:g.43754720T>C	NCBI36
NG_008866.1:g.143541T>C , LRG_766:g.143541T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.904T>C
ENST00000688602.1:c.2301T>C
ENST00000689936.1:c.2273T>C
ENST00000359596.8:c.13968T>C MANE Select	ENSP00000352608.2:p.Phe4656=
ENST00000355481.8:c.13953T>C	ENSP00000347667.3:p.Phe4651=
ENST00000359596.7:c.13968T>C	ENSP00000352608.2:p.Phe4656=
ENST00000360985.7:c.13950T>C	ENSP00000354254.4:p.Phe4650=
ENST00000593677.1:c.428T>C
NM_000540.2:c.13968T>C , LRG_766t1:c.13968T>C	NP_000531.2:p.Phe4656=
NM_001042723.1:c.13953T>C	NP_001036188.1:p.Phe4651=
XM_006723317.1:c.13950T>C	XP_006723380.1:p.Phe4650=
XM_006723319.1:c.13935T>C	XP_006723382.1:p.Phe4645=
XM_011527204.1:c.13965T>C	XP_011525506.1:p.Phe4655=
XM_011527205.1:c.13881T>C	XP_011525507.1:p.Phe4627=
XM_006723317.2:c.13950T>C	XP_006723380.1:p.Phe4650=
XM_006723319.2:c.13935T>C	XP_006723382.1:p.Phe4645=
XM_011527205.2:c.13881T>C	XP_011525507.1:p.Phe4627=
NM_000540.3:c.13968T>C MANE Select	NP_000531.2:p.Phe4656=
NM_001042723.2:c.13953T>C	NP_001036188.1:p.Phe4651=