Canonical Allele Identifier: CA345413271

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947454G>T (hg19) ; chr1:g.237784154G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784154G>T , CM000663.2:g.237784154G>T	GRCh38
NC_000001.10:g.237947454G>T , CM000663.1:g.237947454G>T	GRCh37
NC_000001.9:g.236014077G>T	NCBI36
NG_008799.2:g.746753G>T
NG_008799.3:g.746971G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3534G>T	ENSP00000499659.2:n.*3534G>T
ENST00000659194.3:c.12430G>T	ENSP00000499653.3:p.Val4144Phe
ENST00000660292.2:c.12463G>T	ENSP00000499787.2:p.Val4155Phe
ENST00000659194.2:c.4619G>T
ENST00000366574.7:c.12442G>T MANE Select	ENSP00000355533.2:p.Val4148Phe
ENST00000659194.1:c.4619G>T
ENST00000660292.1:c.2495G>T
ENST00000360064.7:c.12394G>T	ENSP00000353174.7:p.Val4132Phe
ENST00000366574.6:c.12442G>T	ENSP00000355533.2:p.Val4148Phe
ENST00000609119.1:n.3637G>T
NM_001035.2:c.12442G>T	NP_001026.2:p.Val4148Phe
XM_006711802.2:c.12496G>T	XP_006711865.1:p.Val4166Phe
XM_006711803.2:c.12493G>T	XP_006711866.1:p.Val4165Phe
XM_006711804.2:c.12472G>T	XP_006711867.1:p.Val4158Phe
XM_006711805.2:c.12466G>T	XP_006711868.1:p.Val4156Phe
XM_006711806.2:c.12460G>T	XP_006711869.1:p.Val4154Phe
XM_006711807.2:c.12436G>T	XP_006711870.1:p.Val4146Phe
XM_006711808.2:c.12259G>T	XP_006711871.1:p.Val4087Phe
XM_006711810.2:c.12403G>T	XP_006711873.1:p.Val4135Phe
XM_006711802.3:c.12496G>T	XP_006711865.1:p.Val4166Phe
XM_006711803.3:c.12493G>T	XP_006711866.1:p.Val4165Phe
XM_006711804.3:c.12472G>T	XP_006711867.1:p.Val4158Phe
XM_006711805.3:c.12466G>T	XP_006711868.1:p.Val4156Phe
XM_006711806.3:c.12460G>T	XP_006711869.1:p.Val4154Phe
XM_006711807.3:c.12436G>T	XP_006711870.1:p.Val4146Phe
XM_006711808.3:c.12259G>T	XP_006711871.1:p.Val4087Phe
XM_006711810.3:c.12403G>T	XP_006711873.1:p.Val4135Phe
XM_017002028.1:c.12475G>T	XP_016857517.1:p.Val4159Phe
NM_001035.3:c.12442G>T MANE Select	NP_001026.2:p.Val4148Phe