Canonical Allele Identifier: CA405690265

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39075619G>A (hg19) ; chr19:g.38584979G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38584979G>A , CM000681.2:g.38584979G>A	GRCh38
NC_000019.9:g.39075619G>A , CM000681.1:g.39075619G>A	GRCh37
NC_000019.8:g.43767459G>A	NCBI36
NG_008866.1:g.156280G>A , LRG_766:g.156280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1619G>A
ENST00000688602.1:c.3016G>A
ENST00000689936.1:c.2988G>A
ENST00000692547.1:n.76G>A
ENST00000359596.8:c.14683G>A MANE Select	ENSP00000352608.2:p.Gly4895Ser
ENST00000355481.8:c.14668G>A	ENSP00000347667.3:p.Gly4890Ser
ENST00000359596.7:c.14683G>A	ENSP00000352608.2:p.Gly4895Ser
ENST00000360985.7:c.14665G>A	ENSP00000354254.4:p.Gly4889Ser
NM_000540.2:c.14683G>A , LRG_766t1:c.14683G>A	NP_000531.2:p.Gly4895Ser
NM_001042723.1:c.14668G>A	NP_001036188.1:p.Gly4890Ser
XM_006723317.1:c.14665G>A	XP_006723380.1:p.Gly4889Ser
XM_006723319.1:c.14650G>A	XP_006723382.1:p.Gly4884Ser
XM_011527204.1:c.14680G>A	XP_011525506.1:p.Gly4894Ser
XM_011527205.1:c.14596G>A	XP_011525507.1:p.Gly4866Ser
XM_006723317.2:c.14665G>A	XP_006723380.1:p.Gly4889Ser
XM_006723319.2:c.14650G>A	XP_006723382.1:p.Gly4884Ser
XM_011527205.2:c.14596G>A	XP_011525507.1:p.Gly4866Ser
NM_000540.3:c.14683G>A MANE Select	NP_000531.2:p.Gly4895Ser
NM_001042723.2:c.14668G>A	NP_001036188.1:p.Gly4890Ser