Canonical Allele Identifier: CA424051731

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237972269C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237808969C>T , CM000663.2:g.237808969C>T	GRCh38
NC_000001.10:g.237972269C>T , CM000663.1:g.237972269C>T	GRCh37
NC_000001.9:g.236038892C>T	NCBI36
NG_008799.2:g.771568C>T
NG_008799.3:g.771786C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5459C>T	ENSP00000499659.2:n.*5459C>T
ENST00000659194.3:c.14349C>T	ENSP00000499653.3:p.Phe4783=
ENST00000660292.2:c.14388C>T	ENSP00000499787.2:p.Phe4796=
ENST00000659194.2:c.6538C>T
ENST00000366574.7:c.14367C>T MANE Select	ENSP00000355533.2:p.Phe4789=
ENST00000360064.7:c.14316C>T	ENSP00000353174.7:p.Phe4772=
ENST00000366574.6:c.14367C>T	ENSP00000355533.2:p.Phe4789=
ENST00000608590.5:n.878C>T
NM_001035.2:c.14367C>T	NP_001026.2:p.Phe4789=
XM_006711802.2:c.14421C>T	XP_006711865.1:p.Phe4807=
XM_006711803.2:c.14418C>T	XP_006711866.1:p.Phe4806=
XM_006711804.2:c.14397C>T	XP_006711867.1:p.Phe4799=
XM_006711805.2:c.14391C>T	XP_006711868.1:p.Phe4797=
XM_006711806.2:c.14385C>T	XP_006711869.1:p.Phe4795=
XM_006711807.2:c.14361C>T	XP_006711870.1:p.Phe4787=
XM_006711808.2:c.14184C>T	XP_006711871.1:p.Phe4728=
XM_006711810.2:c.14328C>T	XP_006711873.1:p.Phe4776=
XM_006711802.3:c.14421C>T	XP_006711865.1:p.Phe4807=
XM_006711803.3:c.14418C>T	XP_006711866.1:p.Phe4806=
XM_006711804.3:c.14397C>T	XP_006711867.1:p.Phe4799=
XM_006711805.3:c.14391C>T	XP_006711868.1:p.Phe4797=
XM_006711806.3:c.14385C>T	XP_006711869.1:p.Phe4795=
XM_006711807.3:c.14361C>T	XP_006711870.1:p.Phe4787=
XM_006711808.3:c.14184C>T	XP_006711871.1:p.Phe4728=
XM_006711810.3:c.14328C>T	XP_006711873.1:p.Phe4776=
XM_017002028.1:c.14400C>T	XP_016857517.1:p.Phe4800=
NM_001035.3:c.14367C>T MANE Select	NP_001026.2:p.Phe4789=