Canonical Allele Identifier: CA2665100225

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38725388-G-GAAGGGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725388_38725389insAAGGGAT , CM000665.2:g.38725388_38725389insAAGGGAT	GRCh38
NC_000003.11:g.38766879_38766880insAAGGGAT , CM000665.1:g.38766879_38766880insAAGGGAT	GRCh37
NC_000003.10:g.38741883_38741884insAAGGGAT	NCBI36
NG_031891.2:g.73622_73623insATCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3088-75_3088-74insATCCCTT MANE Select	ENSP00000390600.2:n.3088-75_3088-74insATCCCTT
ENST00000643924.1:c.3088-78_3088-77insATCCCTT	ENSP00000495595.1:n.3088-78_3088-77insATCCCTT
ENST00000655275.1:c.3115-78_3115-77insATCCCTT	ENSP00000499510.1:n.3115-78_3115-77insATCCCTT
ENST00000449082.2:c.3088-75_3088-74insATCCCTT	ENSP00000390600.2:n.3088-75_3088-74insATCCCTT
NM_001293306.2:c.3088-78_3088-77insATCCCTT	NP_001280235.2:n.3088-78_3088-77insATCCCTT
NM_001293307.2:c.2794-75_2794-74insATCCCTT	NP_001280236.2:n.2794-75_2794-74insATCCCTT
NM_006514.3:c.3088-75_3088-74insATCCCTT	NP_006505.3:n.3088-75_3088-74insATCCCTT
XM_005265371.2:c.3097-75_3097-74insATCCCTT	XP_005265428.1:n.3097-75_3097-74insATCCCTT
XM_011533993.1:c.3097-78_3097-77insATCCCTT	XP_011532295.1:n.3097-78_3097-77insATCCCTT
XM_011533994.1:c.2803-75_2803-74insATCCCTT	XP_011532296.1:n.2803-75_2803-74insATCCCTT
XM_005265371.3:c.3097-75_3097-74insATCCCTT	XP_005265428.1:n.3097-75_3097-74insATCCCTT
XM_011533993.2:c.3097-78_3097-77insATCCCTT	XP_011532295.1:n.3097-78_3097-77insATCCCTT
XM_011533994.2:c.2803-75_2803-74insATCCCTT	XP_011532296.1:n.2803-75_2803-74insATCCCTT
NM_006514.4:c.3088-75_3088-74insATCCCTT MANE Select	NP_006505.4:n.3088-75_3088-74insATCCCTT