Canonical Allele Identifier: CA1358572599

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38575444_38575446delinsGAC , CM000665.2:g.38575444_38575446delinsGAC	GRCh38
NC_000003.11:g.38616935_38616937delinsGAC , CM000665.1:g.38616935_38616937delinsGAC	GRCh37
NC_000003.10:g.38591939_38591941delinsGAC	NCBI36
NG_008934.1:g.79227_79229delinsGTC , LRG_289:g.79227_79229delinsGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000327956.7:c.3514_3516delinsGTC	ENSP00000333674.7:p.Val1172=
ENST00000333535.9:c.3517_3519delinsGTC	ENSP00000328968.4:p.Val1173=
ENST00000413689.6:c.3517_3519delinsGTC MANE Plus Clinical	ENSP00000410257.1:p.Val1173=
ENST00000423572.7:c.3514_3516delinsGTC MANE Select	ENSP00000398266.2:p.Val1172=
ENST00000333535.8:c.3517_3519delinsGTC	ENSP00000328968.4:p.Val1173=
ENST00000413689.5:c.3517_3519delinsGTC	ENSP00000410257.1:p.Val1173=
ENST00000414099.6:c.3517_3519delinsGTC	ENSP00000398962.2:p.Val1173=
ENST00000423572.6:c.3514_3516delinsGTC	ENSP00000398266.2:p.Val1172=
ENST00000425664.5:c.3517_3519delinsGTC	ENSP00000416634.1:p.Val1173=
ENST00000449557.6:c.3355_3357delinsGTC	ENSP00000413996.2:p.Val1119=
ENST00000450102.6:c.3355_3357delinsGTC	ENSP00000403355.2:p.Val1119=
ENST00000451551.6:c.3355_3357delinsGTC	ENSP00000388797.2:p.Val1119=
ENST00000455624.6:c.3514_3516delinsGTC	ENSP00000399524.2:p.Val1172=
NM_000335.4:c.3514_3516delinsGTC , LRG_289t2:c.3514_3516delinsGTC	NP_000326.2:p.Val1172=
NM_001099404.1:c.3517_3519delinsGTC , LRG_289t3:c.3517_3519delinsGTC	NP_001092874.1:p.Val1173=
NM_001099405.1:c.3517_3519delinsGTC	NP_001092875.1:p.Val1173=
NM_001160160.1:c.3514_3516delinsGTC	NP_001153632.1:p.Val1172=
NM_001160161.1:c.3355_3357delinsGTC	NP_001153633.1:p.Val1119=
NM_198056.2:c.3517_3519delinsGTC , LRG_289t1:c.3517_3519delinsGTC	NP_932173.1:p.Val1173=
XM_006713282.2:c.3517_3519delinsGTC	XP_006713345.1:p.Val1173=
XM_011533991.1:c.3514_3516delinsGTC	XP_011532293.1:p.Val1172=
XM_011533992.1:c.3388_3390delinsGTC	XP_011532294.1:p.Val1130=
NM_001354701.1:c.3514_3516delinsGTC	NP_001341630.1:p.Val1172=
XM_011533991.2:c.3514_3516delinsGTC	XP_011532293.1:p.Val1172=
XM_017007017.1:c.3355_3357delinsGTC	XP_016862506.1:p.Val1119=
NM_000335.5:c.3514_3516delinsGTC MANE Select	NP_000326.2:p.Val1172=
NM_001160160.2:c.3514_3516delinsGTC	NP_001153632.1:p.Val1172=
NM_001354701.2:c.3514_3516delinsGTC	NP_001341630.1:p.Val1172=
NM_001099404.2:c.3517_3519delinsGTC MANE Plus Clinical	NP_001092874.1:p.Val1173=
NM_001099405.2:c.3517_3519delinsGTC	NP_001092875.1:p.Val1173=
NM_001160161.2:c.3355_3357delinsGTC	NP_001153633.1:p.Val1119=
NM_198056.3:c.3517_3519delinsGTC	NP_932173.1:p.Val1173=