Canonical Allele Identifier: CA405682038

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063851T>C (hg19) ; chr19:g.38573211T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573211T>C , CM000681.2:g.38573211T>C	GRCh38
NC_000019.9:g.39063851T>C , CM000681.1:g.39063851T>C	GRCh37
NC_000019.8:g.43755691T>C	NCBI36
NG_008866.1:g.144512T>C , LRG_766:g.144512T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.969T>C
ENST00000688602.1:c.2366T>C
ENST00000689936.1:c.2338T>C
ENST00000359596.8:c.14033T>C MANE Select	ENSP00000352608.2:p.Leu4678Pro
ENST00000355481.8:c.14018T>C	ENSP00000347667.3:p.Leu4673Pro
ENST00000359596.7:c.14033T>C	ENSP00000352608.2:p.Leu4678Pro
ENST00000360985.7:c.14015T>C	ENSP00000354254.4:p.Leu4672Pro
NM_000540.2:c.14033T>C , LRG_766t1:c.14033T>C	NP_000531.2:p.Leu4678Pro
NM_001042723.1:c.14018T>C	NP_001036188.1:p.Leu4673Pro
XM_006723317.1:c.14015T>C	XP_006723380.1:p.Leu4672Pro
XM_006723319.1:c.14000T>C	XP_006723382.1:p.Leu4667Pro
XM_011527204.1:c.14030T>C	XP_011525506.1:p.Leu4677Pro
XM_011527205.1:c.13946T>C	XP_011525507.1:p.Leu4649Pro
XM_006723317.2:c.14015T>C	XP_006723380.1:p.Leu4672Pro
XM_006723319.2:c.14000T>C	XP_006723382.1:p.Leu4667Pro
XM_011527205.2:c.13946T>C	XP_011525507.1:p.Leu4649Pro
NM_000540.3:c.14033T>C MANE Select	NP_000531.2:p.Leu4678Pro
NM_001042723.2:c.14018T>C	NP_001036188.1:p.Leu4673Pro