Canonical Allele Identifier: CA906895448

Gene: SCN11A

Linked Data

• dbSNP Id: rs1182379457
• gnomAD v3: 3-39032564-G-C
• gnomAD v4: 3-39032564-G-C
• MyVariant Identifiers: chr3:g.39074055G>C (hg19) ; chr3:g.39032564G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032564G>C , CM000665.2:g.39032564G>C	GRCh38
NC_000003.11:g.39074055G>C , CM000665.1:g.39074055G>C	GRCh37
NC_000003.10:g.39049059G>C	NCBI36
NG_033859.2:g.24423C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302328.9:c.-403-61C>G MANE Select	ENSP00000307599.3:n.-403-61C>G
ENST00000665106.1:n.82-61C>G
ENST00000668754.1:c.-903-61C>G	ENSP00000499569.1:n.-903-61C>G
ENST00000674755.1:n.233-61C>G
ENST00000675269.1:n.125-61C>G
ENST00000676333.1:n.39-61C>G
XM_011534335.1:c.49-61C>G	XP_011532637.1:n.49-61C>G
XM_011534336.1:c.49-61C>G	XP_011532638.1:n.49-61C>G
XR_940736.1:n.79-61C>G
XR_940737.1:n.79-61C>G
XR_940738.1:n.79-61C>G
XR_940739.1:n.79-61C>G
NM_001349253.1:c.-403-61C>G	NP_001336182.1:n.-403-61C>G
NM_001349253.2:c.-403-61C>G MANE Select	NP_001336182.1:n.-403-61C>G
NR_164473.1:n.85-61C>G