Canonical Allele Identifier: CA15989065

Gene: DSCAM

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.40803034A>G , CM000683.2:g.40803034A>G	GRCh38
NC_000021.8:g.42174960A>G , CM000683.1:g.42174960A>G	GRCh37
NC_000021.7:g.41096830A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400454.6:c.43+43585T>C MANE Select	ENSP00000383303.1:n.43+43585T>C
ENST00000400454.5:c.43+43585T>C	ENSP00000383303.1:n.43+43585T>C
NM_001271534.1:c.43+43585T>C	NP_001258463.1:n.43+43585T>C
NM_001389.3:c.43+43585T>C	NP_001380.2:n.43+43585T>C
NR_073202.1:n.495+43585T>C
XM_011529480.1:c.55+43573T>C	XP_011527782.1:n.55+43573T>C
NM_001271534.2:c.43+43585T>C	NP_001258463.1:n.43+43585T>C
NM_001389.4:c.43+43585T>C	NP_001380.2:n.43+43585T>C
NR_073202.2:n.521+43585T>C
NM_001389.5:c.43+43585T>C MANE Select	NP_001380.2:n.43+43585T>C
NM_001271534.3:c.43+43585T>C	NP_001258463.1:n.43+43585T>C
NR_073202.3:n.540+43585T>C