Canonical Allele Identifier: CA507245126

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063828A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573188A>C , CM000681.2:g.38573188A>C	GRCh38
NC_000019.9:g.39063828A>C , CM000681.1:g.39063828A>C	GRCh37
NC_000019.8:g.43755668A>C	NCBI36
NG_008866.1:g.144489A>C , LRG_766:g.144489A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.946A>C
ENST00000688602.1:c.2343A>C
ENST00000689936.1:c.2315A>C
ENST00000359596.8:c.14010A>C MANE Select	ENSP00000352608.2:p.Val4670=
ENST00000355481.8:c.13995A>C	ENSP00000347667.3:p.Val4665=
ENST00000359596.7:c.14010A>C	ENSP00000352608.2:p.Val4670=
ENST00000360985.7:c.13992A>C	ENSP00000354254.4:p.Val4664=
NM_000540.2:c.14010A>C , LRG_766t1:c.14010A>C	NP_000531.2:p.Val4670=
NM_001042723.1:c.13995A>C	NP_001036188.1:p.Val4665=
XM_006723317.1:c.13992A>C	XP_006723380.1:p.Val4664=
XM_006723319.1:c.13977A>C	XP_006723382.1:p.Val4659=
XM_011527204.1:c.14007A>C	XP_011525506.1:p.Val4669=
XM_011527205.1:c.13923A>C	XP_011525507.1:p.Val4641=
XM_006723317.2:c.13992A>C	XP_006723380.1:p.Val4664=
XM_006723319.2:c.13977A>C	XP_006723382.1:p.Val4659=
XM_011527205.2:c.13923A>C	XP_011525507.1:p.Val4641=
NM_000540.3:c.14010A>C MANE Select	NP_000531.2:p.Val4670=
NM_001042723.2:c.13995A>C	NP_001036188.1:p.Val4665=