Canonical Allele Identifier: CA2389652938

Gene: DSCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.40043117T= , CM000683.2:g.40043117T=	GRCh38
NC_000021.8:g.41415044T= , CM000683.1:g.41415044T=	GRCh37
NC_000021.7:g.40336914T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001389.5:c.5384-444A= MANE Select	NP_001380.2:n.5384-444A=
ENST00000400454.6:c.5384-444A= MANE Select	ENSP00000383303.1:n.5384-444A=
NM_001271534.1:c.5384-444A=	NP_001258463.1:n.5384-444A=
NM_001271534.2:c.5384-444A=	NP_001258463.1:n.5384-444A=
NM_001271534.3:c.5384-444A=	NP_001258463.1:n.5384-444A=
NM_001389.3:c.5384-444A=	NP_001380.2:n.5384-444A=
NM_001389.4:c.5384-444A=	NP_001380.2:n.5384-444A=
NR_073202.1:n.5645-444A=
NR_073202.2:n.5671-444A=
NR_073202.3:n.5690-444A=
ENST00000400454.5:c.5384-444A=	ENSP00000383303.1:n.5384-444A=
ENST00000404019.2:c.4640-444A=	ENSP00000385342.2:n.4640-444A=
ENST00000617870.4:c.4889-444A=	ENSP00000478698.1:n.4889-444A=
XM_011529481.1:c.3020-444A=	XP_011527783.1:n.3020-444A=
XM_017028281.1:c.4676-444A=	XP_016883770.1:n.4676-444A=