Canonical Allele Identifier: CA345424319
Gene: RYR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237808975A>T , CM000663.2:g.237808975A>T GRCh38
NC_000001.10:g.237972275A>T , CM000663.1:g.237972275A>T GRCh37
NC_000001.9:g.236038898A>T NCBI36
NG_008799.2:g.771574A>T
NG_008799.3:g.771792A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.*5465A>T ENSP00000499659.2:n.*5465A>T
ENST00000659194.3:c.14355A>T ENSP00000499653.3:p.Lys4785Asn
ENST00000660292.2:c.14394A>T ENSP00000499787.2:p.Lys4798Asn
ENST00000659194.2:c.6544A>T
ENST00000366574.7:c.14373A>T MANE Select ENSP00000355533.2:p.Lys4791Asn
ENST00000360064.7:c.14322A>T ENSP00000353174.7:p.Lys4774Asn
ENST00000366574.6:c.14373A>T ENSP00000355533.2:p.Lys4791Asn
ENST00000608590.5:n.884A>T
NM_001035.2:c.14373A>T NP_001026.2:p.Lys4791Asn
XM_006711802.2:c.14427A>T XP_006711865.1:p.Lys4809Asn
XM_006711803.2:c.14424A>T XP_006711866.1:p.Lys4808Asn
XM_006711804.2:c.14403A>T XP_006711867.1:p.Lys4801Asn
XM_006711805.2:c.14397A>T XP_006711868.1:p.Lys4799Asn
XM_006711806.2:c.14391A>T XP_006711869.1:p.Lys4797Asn
XM_006711807.2:c.14367A>T XP_006711870.1:p.Lys4789Asn
XM_006711808.2:c.14190A>T XP_006711871.1:p.Lys4730Asn
XM_006711810.2:c.14334A>T XP_006711873.1:p.Lys4778Asn
XM_006711802.3:c.14427A>T XP_006711865.1:p.Lys4809Asn
XM_006711803.3:c.14424A>T XP_006711866.1:p.Lys4808Asn
XM_006711804.3:c.14403A>T XP_006711867.1:p.Lys4801Asn
XM_006711805.3:c.14397A>T XP_006711868.1:p.Lys4799Asn
XM_006711806.3:c.14391A>T XP_006711869.1:p.Lys4797Asn
XM_006711807.3:c.14367A>T XP_006711870.1:p.Lys4789Asn
XM_006711808.3:c.14190A>T XP_006711871.1:p.Lys4730Asn
XM_006711810.3:c.14334A>T XP_006711873.1:p.Lys4778Asn
XM_017002028.1:c.14406A>T XP_016857517.1:p.Lys4802Asn
NM_001035.3:c.14373A>T MANE Select NP_001026.2:p.Lys4791Asn