Canonical Allele Identifier: CA405681988

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063847G>C (hg19) ; chr19:g.38573207G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573207G>C , CM000681.2:g.38573207G>C	GRCh38
NC_000019.9:g.39063847G>C , CM000681.1:g.39063847G>C	GRCh37
NC_000019.8:g.43755687G>C	NCBI36
NG_008866.1:g.144508G>C , LRG_766:g.144508G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.965G>C
ENST00000688602.1:c.2362G>C
ENST00000689936.1:c.2334G>C
ENST00000359596.8:c.14029G>C MANE Select	ENSP00000352608.2:p.Glu4677Gln
ENST00000355481.8:c.14014G>C	ENSP00000347667.3:p.Glu4672Gln
ENST00000359596.7:c.14029G>C	ENSP00000352608.2:p.Glu4677Gln
ENST00000360985.7:c.14011G>C	ENSP00000354254.4:p.Glu4671Gln
NM_000540.2:c.14029G>C , LRG_766t1:c.14029G>C	NP_000531.2:p.Glu4677Gln
NM_001042723.1:c.14014G>C	NP_001036188.1:p.Glu4672Gln
XM_006723317.1:c.14011G>C	XP_006723380.1:p.Glu4671Gln
XM_006723319.1:c.13996G>C	XP_006723382.1:p.Glu4666Gln
XM_011527204.1:c.14026G>C	XP_011525506.1:p.Glu4676Gln
XM_011527205.1:c.13942G>C	XP_011525507.1:p.Glu4648Gln
XM_006723317.2:c.14011G>C	XP_006723380.1:p.Glu4671Gln
XM_006723319.2:c.13996G>C	XP_006723382.1:p.Glu4666Gln
XM_011527205.2:c.13942G>C	XP_011525507.1:p.Glu4648Gln
NM_000540.3:c.14029G>C MANE Select	NP_000531.2:p.Glu4677Gln
NM_001042723.2:c.14014G>C	NP_001036188.1:p.Glu4672Gln