Canonical Allele Identifier: CA349025051

Gene: SCN3A

Linked Data

• ClinVar Variation Id: 2744542
• ClinVar RCV Id: RCV003562881
• COSMIC: COSM370032
• MyVariant Identifiers: chr2:g.165953800C>T (hg19) ; chr2:g.165097290C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165097290C>T , CM000664.2:g.165097290C>T	GRCh38
NC_000002.11:g.165953800C>T , CM000664.1:g.165953800C>T	GRCh37
NC_000002.10:g.165662046C>T	NCBI36
NG_042289.1:g.111799G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706067.1:c.4150G>A	ENSP00000516211.1:p.Asp1384Asn
ENST00000283254.12:c.4201G>A MANE Select	ENSP00000283254.7:p.Asp1401Asn
ENST00000638473.1:c.*2042G>A	ENSP00000491552.1:n.*2042G>A
ENST00000639244.1:c.4150G>A	ENSP00000492251.1:p.Asp1384Asn
ENST00000640652.1:c.*935G>A	ENSP00000492807.1:n.*935G>A
ENST00000658209.1:c.2410G>A	ENSP00000499598.1:n.2410G>A
ENST00000283254.11:c.4201G>A	ENSP00000283254.7:p.Asp1401Asn
ENST00000360093.7:c.4201G>A	ENSP00000353206.3:p.Asp1401Asn
ENST00000409101.7:c.4054G>A	ENSP00000386726.3:p.Asp1352Asn
ENST00000440431.6:c.4054G>A	ENSP00000403348.1:p.Asp1352Asn
ENST00000471697.1:n.325G>A
NM_001081676.1:c.4054G>A	NP_001075145.1:p.Asp1352Asn
NM_001081677.1:c.4054G>A	NP_001075146.1:p.Asp1352Asn
NM_006922.3:c.4201G>A	NP_008853.3:p.Asp1401Asn
XM_006712679.1:c.4201G>A	XP_006712742.1:p.Asp1401Asn
XM_011511610.1:c.4201G>A	XP_011509912.1:p.Asp1401Asn
XM_011511611.1:c.4201G>A	XP_011509913.1:p.Asp1401Asn
XM_011511612.1:c.4150G>A	XP_011509914.1:p.Asp1384Asn
XM_011511613.1:c.2311G>A	XP_011509915.1:p.Asp771Asn
XM_011511610.3:c.4201G>A	XP_011509912.1:p.Asp1401Asn
XM_011511613.3:c.2311G>A	XP_011509915.1:p.Asp771Asn
XM_017004660.2:c.4201G>A	XP_016860149.1:p.Asp1401Asn
XM_017004661.2:c.4150G>A	XP_016860150.1:p.Asp1384Asn
XM_017004662.2:c.4063G>A	XP_016860151.1:p.Asp1355Asn
XM_017004663.2:c.2311G>A	XP_016860152.1:p.Asp771Asn
NM_006922.4:c.4201G>A MANE Select	NP_008853.3:p.Asp1401Asn
NM_001081676.2:c.4054G>A	NP_001075145.1:p.Asp1352Asn
NM_001081677.2:c.4054G>A	NP_001075146.1:p.Asp1352Asn