Canonical Allele Identifier: CA507355086

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38561253C>T , CM000681.2:g.38561253C>T	GRCh38
NC_000019.9:g.39051893C>T , CM000681.1:g.39051893C>T	GRCh37
NC_000019.8:g.43743733C>T	NCBI36
NG_008866.1:g.132554C>T , LRG_766:g.132554C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.12423C>T MANE Select	NP_000531.2:p.Asn4141=
ENST00000359596.8:c.12423C>T MANE Select	ENSP00000352608.2:p.Asn4141=
NM_000540.2:c.12423C>T , LRG_766t1:c.12423C>T	NP_000531.2:p.Asn4141=
NM_001042723.1:c.12408C>T	NP_001036188.1:p.Asn4136=
NM_001042723.2:c.12408C>T	NP_001036188.1:p.Asn4136=
ENST00000355481.8:c.12408C>T	ENSP00000347667.3:p.Asn4136=
ENST00000359596.7:c.12423C>T	ENSP00000352608.2:p.Asn4141=
ENST00000360985.7:c.12405C>T	ENSP00000354254.4:p.Asn4135=
ENST00000594335.5:c.5792C>T
ENST00000688602.1:c.833C>T
ENST00000689936.1:c.815C>T
XM_006723317.1:c.12405C>T	XP_006723380.1:p.Asn4135=
XM_006723317.2:c.12405C>T	XP_006723380.1:p.Asn4135=
XM_006723319.1:c.12390C>T	XP_006723382.1:p.Asn4130=
XM_006723319.2:c.12390C>T	XP_006723382.1:p.Asn4130=
XM_011527204.1:c.12420C>T	XP_011525506.1:p.Asn4140=
XM_011527205.1:c.12423C>T	XP_011525507.1:p.Asn4141=
XM_011527205.2:c.12423C>T	XP_011525507.1:p.Asn4141=