Canonical Allele Identifier: CA2390045126

Gene: DSCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.40845029C= , CM000683.2:g.40845029C=	GRCh38
NC_000021.8:g.42216955C= , CM000683.1:g.42216955C=	GRCh37
NC_000021.7:g.41138825C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001389.5:c.43+1590G= MANE Select	NP_001380.2:n.43+1590G=
ENST00000400454.6:c.43+1590G= MANE Select	ENSP00000383303.1:n.43+1590G=
NM_001271534.1:c.43+1590G=	NP_001258463.1:n.43+1590G=
NM_001271534.2:c.43+1590G=	NP_001258463.1:n.43+1590G=
NM_001271534.3:c.43+1590G=	NP_001258463.1:n.43+1590G=
NM_001389.3:c.43+1590G=	NP_001380.2:n.43+1590G=
NM_001389.4:c.43+1590G=	NP_001380.2:n.43+1590G=
NR_073202.1:n.495+1590G=
NR_073202.2:n.521+1590G=
NR_073202.3:n.540+1590G=
ENST00000400454.5:c.43+1590G=	ENSP00000383303.1:n.43+1590G=
XM_011529480.1:c.55+1578G=	XP_011527782.1:n.55+1578G=