Canonical Allele Identifier: CA405687013

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39070671A>C (hg19) ; chr19:g.38580031A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580031A>C , CM000681.2:g.38580031A>C	GRCh38
NC_000019.9:g.39070671A>C , CM000681.1:g.39070671A>C	GRCh37
NC_000019.8:g.43762511A>C	NCBI36
NG_008866.1:g.151332A>C , LRG_766:g.151332A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1350A>C
ENST00000688602.1:c.2747A>C
ENST00000689936.1:c.2719A>C
ENST00000359596.8:c.14414A>C MANE Select	ENSP00000352608.2:p.Tyr4805Ser
ENST00000355481.8:c.14399A>C	ENSP00000347667.3:p.Tyr4800Ser
ENST00000359596.7:c.14414A>C	ENSP00000352608.2:p.Tyr4805Ser
ENST00000360985.7:c.14396A>C	ENSP00000354254.4:p.Tyr4799Ser
NM_000540.2:c.14414A>C , LRG_766t1:c.14414A>C	NP_000531.2:p.Tyr4805Ser
NM_001042723.1:c.14399A>C	NP_001036188.1:p.Tyr4800Ser
XM_006723317.1:c.14396A>C	XP_006723380.1:p.Tyr4799Ser
XM_006723319.1:c.14381A>C	XP_006723382.1:p.Tyr4794Ser
XM_011527204.1:c.14411A>C	XP_011525506.1:p.Tyr4804Ser
XM_011527205.1:c.14327A>C	XP_011525507.1:p.Tyr4776Ser
XM_006723317.2:c.14396A>C	XP_006723380.1:p.Tyr4799Ser
XM_006723319.2:c.14381A>C	XP_006723382.1:p.Tyr4794Ser
XM_011527205.2:c.14327A>C	XP_011525507.1:p.Tyr4776Ser
NM_000540.3:c.14414A>C MANE Select	NP_000531.2:p.Tyr4805Ser
NM_001042723.2:c.14399A>C	NP_001036188.1:p.Tyr4800Ser