Canonical Allele Identifier: CA507356098

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071051G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580411G>T , CM000681.2:g.38580411G>T	GRCh38
NC_000019.9:g.39071051G>T , CM000681.1:g.39071051G>T	GRCh37
NC_000019.8:g.43762891G>T	NCBI36
NG_008866.1:g.151712G>T , LRG_766:g.151712G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1489G>T
ENST00000688602.1:c.2886G>T
ENST00000689936.1:c.2858G>T
ENST00000359596.8:c.14553G>T MANE Select	ENSP00000352608.2:p.Leu4851=
ENST00000355481.8:c.14538G>T	ENSP00000347667.3:p.Leu4846=
ENST00000359596.7:c.14553G>T	ENSP00000352608.2:p.Leu4851=
ENST00000360985.7:c.14535G>T	ENSP00000354254.4:p.Leu4845=
NM_000540.2:c.14553G>T , LRG_766t1:c.14553G>T	NP_000531.2:p.Leu4851=
NM_001042723.1:c.14538G>T	NP_001036188.1:p.Leu4846=
XM_006723317.1:c.14535G>T	XP_006723380.1:p.Leu4845=
XM_006723319.1:c.14520G>T	XP_006723382.1:p.Leu4840=
XM_011527204.1:c.14550G>T	XP_011525506.1:p.Leu4850=
XM_011527205.1:c.14466G>T	XP_011525507.1:p.Leu4822=
XM_006723317.2:c.14535G>T	XP_006723380.1:p.Leu4845=
XM_006723319.2:c.14520G>T	XP_006723382.1:p.Leu4840=
XM_011527205.2:c.14466G>T	XP_011525507.1:p.Leu4822=
NM_000540.3:c.14553G>T MANE Select	NP_000531.2:p.Leu4851=
NM_001042723.2:c.14538G>T	NP_001036188.1:p.Leu4846=