Canonical Allele Identifier: CA507241584

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.38937397A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38446757A>T , CM000681.2:g.38446757A>T	GRCh38
NC_000019.9:g.38937397A>T , CM000681.1:g.38937397A>T	GRCh37
NC_000019.8:g.43629237A>T	NCBI36
NG_008866.1:g.18058A>T , LRG_766:g.18058A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.789A>T	ENSP00000471601.2:p.Pro263=
ENST00000359596.8:c.789A>T MANE Select	ENSP00000352608.2:p.Pro263=
ENST00000355481.8:c.789A>T	ENSP00000347667.3:p.Pro263=
ENST00000359596.7:c.789A>T	ENSP00000352608.2:p.Pro263=
ENST00000360985.7:c.789A>T	ENSP00000354254.4:p.Pro263=
NM_000540.2:c.789A>T , LRG_766t1:c.789A>T	NP_000531.2:p.Pro263=
NM_001042723.1:c.789A>T	NP_001036188.1:p.Pro263=
XM_006723317.1:c.789A>T	XP_006723380.1:p.Pro263=
XM_006723319.1:c.789A>T	XP_006723382.1:p.Pro263=
XM_011527204.1:c.789A>T	XP_011525506.1:p.Pro263=
XM_011527205.1:c.789A>T	XP_011525507.1:p.Pro263=
XM_006723317.2:c.789A>T	XP_006723380.1:p.Pro263=
XM_006723319.2:c.789A>T	XP_006723382.1:p.Pro263=
XM_011527205.2:c.789A>T	XP_011525507.1:p.Pro263=
XR_001753735.1:n.872A>T
NM_000540.3:c.789A>T MANE Select	NP_000531.2:p.Pro263=
NM_001042723.2:c.789A>T	NP_001036188.1:p.Pro263=