Canonical Allele Identifier: CA429972451
Gene: SCN2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.166243291C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165386781C>A , CM000664.2:g.165386781C>A GRCh38
NC_000002.11:g.166243291C>A , CM000664.1:g.166243291C>A GRCh37
NC_000002.10:g.165951537C>A NCBI36
NG_008143.1:g.152380C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000631182.3:c.4587C>A MANE Plus Clinical ENSP00000486885.1:p.Thr1529=
ENST00000375437.7:c.4587C>A MANE Select ENSP00000364586.2:p.Thr1529=
ENST00000636071.2:c.4587C>A ENSP00000490107.1:p.Thr1529=
ENST00000636135.1:c.*2906C>A ENSP00000489821.1:n.*2906C>A
ENST00000636384.2:c.*2574C>A ENSP00000490765.1:n.*2574C>A
ENST00000636662.2:c.*5110C>A ENSP00000489873.1:n.*5110C>A
ENST00000636769.1:c.*2529C>A ENSP00000490800.1:n.*2529C>A
ENST00000636985.2:c.4191C>A ENSP00000490849.1:p.Thr1397=
ENST00000637266.2:c.4587C>A ENSP00000490866.1:p.Thr1529=
ENST00000283256.10:c.4587C>A ENSP00000283256.6:p.Thr1529=
ENST00000375427.4:c.4587C>A ENSP00000364576.2:p.Thr1529=
ENST00000375437.6:c.4587C>A ENSP00000364586.2:p.Thr1529=
ENST00000480032.4:n.8018C>A
ENST00000631182.2:c.4587C>A ENSP00000486885.1:p.Thr1529=
NM_001040142.1:c.4587C>A NP_001035232.1:p.Thr1529=
NM_001040143.1:c.4587C>A NP_001035233.1:p.Thr1529=
NM_021007.2:c.4587C>A NP_066287.2:p.Thr1529=
XM_005246750.2:c.4587C>A XP_005246807.1:p.Thr1529=
XM_005246753.2:c.4587C>A XP_005246810.1:p.Thr1529=
XM_005246754.3:c.4557C>A XP_005246811.1:p.Thr1519=
XM_005246755.3:c.3834C>A XP_005246812.1:p.Thr1278=
XM_011511608.1:c.4587C>A XP_011509910.1:p.Thr1529=
XM_011511609.1:c.4587C>A XP_011509911.1:p.Thr1529=
XM_005246753.3:c.4587C>A XP_005246810.1:p.Thr1529=
XM_017004656.1:c.4587C>A XP_016860145.1:p.Thr1529=
XM_017004657.1:c.4587C>A XP_016860146.1:p.Thr1529=
XM_017004658.1:c.3834C>A XP_016860147.1:p.Thr1278=
XM_017004659.1:c.2385C>A XP_016860148.1:p.Thr795=
XM_024453037.1:c.3834C>A XP_024308805.1:p.Thr1278=
NM_001040142.2:c.4587C>A MANE Select NP_001035232.1:p.Thr1529=
NM_001040143.2:c.4587C>A NP_001035233.1:p.Thr1529=
NM_001371246.1:c.4587C>A MANE Plus Clinical NP_001358175.1:p.Thr1529=
NM_001371247.1:c.4587C>A NP_001358176.1:p.Thr1529=
NM_021007.3:c.4587C>A NP_066287.2:p.Thr1529=