Canonical Allele Identifier: CA1358718358

Gene: SCN11A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38895058_38895060delinsCAG , CM000665.2:g.38895058_38895060delinsCAG	GRCh38
NC_000003.11:g.38936549_38936551delinsCAG , CM000665.1:g.38936549_38936551delinsCAG	GRCh37
NC_000003.10:g.38911553_38911555delinsCAG	NCBI36
NG_033859.1:g.60502_60504delinsCTG
NG_033859.2:g.161927_161929delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.2404-96_2404-94delinsCTG MANE Select	ENSP00000307599.3:n.2404-96_2404-94delinsCTG
ENST00000668754.1:c.2404-96_2404-94delinsCTG	ENSP00000499569.1:n.2404-96_2404-94delinsCTG
ENST00000675223.1:c.2404-96_2404-94delinsCTG	ENSP00000502481.1:n.2404-96_2404-94delinsCTG
ENST00000675672.1:c.2404-96_2404-94delinsCTG	ENSP00000502446.1:n.2404-96_2404-94delinsCTG
ENST00000675892.1:c.2224-96_2224-94delinsCTG	ENSP00000502318.1:n.2224-96_2224-94delinsCTG
ENST00000676045.1:c.2448-96_2448-94delinsCTG	ENSP00000501685.1:n.2448-96_2448-94delinsCTG
ENST00000676176.1:c.2023-96_2023-94delinsCTG	ENSP00000501891.1:n.2023-96_2023-94delinsCTG
ENST00000302328.7:c.2404-96_2404-94delinsCTG	ENSP00000307599.3:n.2404-96_2404-94delinsCTG
ENST00000444237.2:c.2404-96_2404-94delinsCTG	ENSP00000408028.2:n.2404-96_2404-94delinsCTG
ENST00000456224.7:c.2404-96_2404-94delinsCTG	ENSP00000416757.3:n.2404-96_2404-94delinsCTG
NM_001287223.1:c.2404-96_2404-94delinsCTG	NP_001274152.1:n.2404-96_2404-94delinsCTG
NM_014139.2:c.2404-96_2404-94delinsCTG	NP_054858.2:n.2404-96_2404-94delinsCTG
XM_011533320.1:c.2404-96_2404-94delinsCTG	XP_011531622.1:n.2404-96_2404-94delinsCTG
XM_011533321.1:c.1741-96_1741-94delinsCTG	XP_011531623.1:n.1741-96_1741-94delinsCTG
XM_011533322.1:c.952-96_952-94delinsCTG	XP_011531624.1:n.952-96_952-94delinsCTG
NM_001349253.1:c.2404-96_2404-94delinsCTG	NP_001336182.1:n.2404-96_2404-94delinsCTG
XM_011533321.2:c.1741-96_1741-94delinsCTG	XP_011531623.1:n.1741-96_1741-94delinsCTG
XM_017005647.1:c.2779-96_2779-94delinsCTG	XP_016861136.1:n.2779-96_2779-94delinsCTG
XM_017005648.1:c.2206-96_2206-94delinsCTG	XP_016861137.1:n.2206-96_2206-94delinsCTG
XM_017005650.1:c.2404-96_2404-94delinsCTG	XP_016861139.1:n.2404-96_2404-94delinsCTG
XM_017005651.1:c.2131-96_2131-94delinsCTG	XP_016861140.1:n.2131-96_2131-94delinsCTG
XM_017005652.1:c.2404-96_2404-94delinsCTG	XP_016861141.1:n.2404-96_2404-94delinsCTG
XM_017005653.1:c.808-96_808-94delinsCTG	XP_016861142.1:n.808-96_808-94delinsCTG
NM_001349253.2:c.2404-96_2404-94delinsCTG MANE Select	NP_001336182.1:n.2404-96_2404-94delinsCTG
NM_014139.3:c.2404-96_2404-94delinsCTG	NP_054858.2:n.2404-96_2404-94delinsCTG