Canonical Allele Identifier: CA405681992

Gene: RYR1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.965G>T
ENST00000688602.1:c.2362G>T
ENST00000689936.1:c.2334G>T
ENST00000359596.8:c.14029G>T MANE Select	ENSP00000352608.2:p.Glu4677Ter
ENST00000355481.8:c.14014G>T	ENSP00000347667.3:p.Glu4672Ter
ENST00000359596.7:c.14029G>T	ENSP00000352608.2:p.Glu4677Ter
ENST00000360985.7:c.14011G>T	ENSP00000354254.4:p.Glu4671Ter
NM_000540.2:c.14029G>T , LRG_766t1:c.14029G>T	NP_000531.2:p.Glu4677Ter
NM_001042723.1:c.14014G>T	NP_001036188.1:p.Glu4672Ter
XM_006723317.1:c.14011G>T	XP_006723380.1:p.Glu4671Ter
XM_006723319.1:c.13996G>T	XP_006723382.1:p.Glu4666Ter
XM_011527204.1:c.14026G>T	XP_011525506.1:p.Glu4676Ter
XM_011527205.1:c.13942G>T	XP_011525507.1:p.Glu4648Ter
XM_006723317.2:c.14011G>T	XP_006723380.1:p.Glu4671Ter
XM_006723319.2:c.13996G>T	XP_006723382.1:p.Glu4666Ter
XM_011527205.2:c.13942G>T	XP_011525507.1:p.Glu4648Ter
NM_000540.3:c.14029G>T MANE Select	NP_000531.2:p.Glu4677Ter
NM_001042723.2:c.14014G>T	NP_001036188.1:p.Glu4672Ter