Canonical Allele Identifier: CA405673557

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39056093G>T (hg19) ; chr19:g.38565453G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565453G>T , CM000681.2:g.38565453G>T	GRCh38
NC_000019.9:g.39056093G>T , CM000681.1:g.39056093G>T	GRCh37
NC_000019.8:g.43747933G>T	NCBI36
NG_008866.1:g.136754G>T , LRG_766:g.136754G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.55G>T
ENST00000688602.1:c.1529G>T
ENST00000689936.1:c.1511G>T
ENST00000359596.8:c.13119G>T MANE Select	ENSP00000352608.2:p.Lys4373Asn
ENST00000355481.8:c.13104G>T	ENSP00000347667.3:p.Lys4368Asn
ENST00000359596.7:c.13119G>T	ENSP00000352608.2:p.Lys4373Asn
ENST00000360985.7:c.13101G>T	ENSP00000354254.4:p.Lys4367Asn
NM_000540.2:c.13119G>T , LRG_766t1:c.13119G>T	NP_000531.2:p.Lys4373Asn
NM_001042723.1:c.13104G>T	NP_001036188.1:p.Lys4368Asn
XM_006723317.1:c.13101G>T	XP_006723380.1:p.Lys4367Asn
XM_006723319.1:c.13086G>T	XP_006723382.1:p.Lys4362Asn
XM_011527204.1:c.13116G>T	XP_011525506.1:p.Lys4372Asn
XM_011527205.1:c.13119G>T	XP_011525507.1:p.Lys4373Asn
XM_006723317.2:c.13101G>T	XP_006723380.1:p.Lys4367Asn
XM_006723319.2:c.13086G>T	XP_006723382.1:p.Lys4362Asn
XM_011527205.2:c.13119G>T	XP_011525507.1:p.Lys4373Asn
NM_000540.3:c.13119G>T MANE Select	NP_000531.2:p.Lys4373Asn
NM_001042723.2:c.13104G>T	NP_001036188.1:p.Lys4368Asn