Canonical Allele Identifier: CA405681845

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063830T>C (hg19) ; chr19:g.38573190T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573190T>C , CM000681.2:g.38573190T>C	GRCh38
NC_000019.9:g.39063830T>C , CM000681.1:g.39063830T>C	GRCh37
NC_000019.8:g.43755670T>C	NCBI36
NG_008866.1:g.144491T>C , LRG_766:g.144491T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.948T>C
ENST00000688602.1:c.2345T>C
ENST00000689936.1:c.2317T>C
ENST00000359596.8:c.14012T>C MANE Select	ENSP00000352608.2:p.Ile4671Thr
ENST00000355481.8:c.13997T>C	ENSP00000347667.3:p.Ile4666Thr
ENST00000359596.7:c.14012T>C	ENSP00000352608.2:p.Ile4671Thr
ENST00000360985.7:c.13994T>C	ENSP00000354254.4:p.Ile4665Thr
NM_000540.2:c.14012T>C , LRG_766t1:c.14012T>C	NP_000531.2:p.Ile4671Thr
NM_001042723.1:c.13997T>C	NP_001036188.1:p.Ile4666Thr
XM_006723317.1:c.13994T>C	XP_006723380.1:p.Ile4665Thr
XM_006723319.1:c.13979T>C	XP_006723382.1:p.Ile4660Thr
XM_011527204.1:c.14009T>C	XP_011525506.1:p.Ile4670Thr
XM_011527205.1:c.13925T>C	XP_011525507.1:p.Ile4642Thr
XM_006723317.2:c.13994T>C	XP_006723380.1:p.Ile4665Thr
XM_006723319.2:c.13979T>C	XP_006723382.1:p.Ile4660Thr
XM_011527205.2:c.13925T>C	XP_011525507.1:p.Ile4642Thr
NM_000540.3:c.14012T>C MANE Select	NP_000531.2:p.Ile4671Thr
NM_001042723.2:c.13997T>C	NP_001036188.1:p.Ile4666Thr