Canonical Allele Identifier: CA2389790100

Gene: DSCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.40331020C= , CM000683.2:g.40331020C=	GRCh38
NC_000021.8:g.41702947C= , CM000683.1:g.41702947C=	GRCh37
NC_000021.7:g.40624817C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001389.5:c.1783+7081G= MANE Select	NP_001380.2:n.1783+7081G=
ENST00000400454.6:c.1783+7081G= MANE Select	ENSP00000383303.1:n.1783+7081G=
NM_001271534.1:c.1783+7081G=	NP_001258463.1:n.1783+7081G=
NM_001271534.2:c.1783+7081G=	NP_001258463.1:n.1783+7081G=
NM_001271534.3:c.1783+7081G=	NP_001258463.1:n.1783+7081G=
NM_001389.3:c.1783+7081G=	NP_001380.2:n.1783+7081G=
NM_001389.4:c.1783+7081G=	NP_001380.2:n.1783+7081G=
NR_073202.1:n.2235+7081G=
NR_073202.2:n.2261+7081G=
NR_073202.3:n.2280+7081G=
ENST00000400454.5:c.1783+7081G=	ENSP00000383303.1:n.1783+7081G=
ENST00000404019.2:c.1039+7081G=	ENSP00000385342.2:n.1039+7081G=
ENST00000617870.4:c.1288+7081G=	ENSP00000478698.1:n.1288+7081G=
XM_011529480.1:c.1795+7081G=	XP_011527782.1:n.1795+7081G=
XM_017028281.1:c.1075+7081G=	XP_016883770.1:n.1075+7081G=