Canonical Allele Identifier: CA10637697

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118135617G>A , CM000673.2:g.118135617G>A	GRCh38
NC_000011.9:g.118006332G>A , CM000673.1:g.118006332G>A	GRCh37
NC_000011.8:g.117511542G>A	NCBI36
NG_011710.1:g.22299C>T , LRG_330:g.22299C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_174934.4:c.*1410C>T MANE Select	NP_777594.1:n.*1410C>T
ENST00000324727.9:c.*1410C>T MANE Select	ENSP00000322460.4:n.*1410C>T
NM_001142348.1:c.*1410C>T	NP_001135820.1:n.*1410C>T
NM_001142348.2:c.*1410C>T	NP_001135820.1:n.*1410C>T
NM_001142349.1:c.*1410C>T	NP_001135821.1:n.*1410C>T
NM_001142349.2:c.*1410C>T	NP_001135821.1:n.*1410C>T
NM_174934.3:c.*1410C>T , LRG_330t1:c.*1410C>T	NP_777594.1:n.*1410C>T
NR_024527.1:n.2122C>T
NR_024527.2:n.2086C>T
ENST00000324727.8:c.*1410C>T	ENSP00000322460.4:n.*1410C>T
ENST00000415030.6:n.2240C>T
ENST00000423160.2:n.1731C>T