Canonical Allele Identifier: CA2389881516

Gene: DSCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.40514656T= , CM000683.2:g.40514656T=	GRCh38
NC_000021.8:g.41886583T= , CM000683.1:g.41886583T=	GRCh37
NC_000021.7:g.40808453T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001389.5:c.509-145411A= MANE Select	NP_001380.2:n.509-145411A=
ENST00000400454.6:c.509-145411A= MANE Select	ENSP00000383303.1:n.509-145411A=
NM_001271534.1:c.509-145411A=	NP_001258463.1:n.509-145411A=
NM_001271534.2:c.509-145411A=	NP_001258463.1:n.509-145411A=
NM_001271534.3:c.509-145411A=	NP_001258463.1:n.509-145411A=
NM_001389.3:c.509-145411A=	NP_001380.2:n.509-145411A=
NM_001389.4:c.509-145411A=	NP_001380.2:n.509-145411A=
NR_073202.1:n.961-145411A=
NR_073202.2:n.987-145411A=
NR_073202.3:n.1006-145411A=
ENST00000400454.5:c.509-145411A=	ENSP00000383303.1:n.509-145411A=
XM_011529480.1:c.521-145411A=	XP_011527782.1:n.521-145411A=