Canonical Allele Identifier: CA719961735

Gene: ITGAD

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31399864C>G , CM000678.2:g.31399864C>G	GRCh38
NC_000016.9:g.31411185C>G , CM000678.1:g.31411185C>G	GRCh37
NC_000016.8:g.31318686C>G	NCBI36
NG_050624.1:g.11624C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389202.3:c.427+1955C>G MANE Select	ENSP00000373854.2:n.427+1955C>G
ENST00000389202.2:c.427+1955C>G	ENSP00000373854.2:n.427+1955C>G
ENST00000444228.2:n.453+1955C>G
NM_005353.2:c.427+1955C>G	NP_005344.2:n.427+1955C>G
XM_011545835.1:c.427+1955C>G	XP_011544137.1:n.427+1955C>G
XM_011545836.1:c.427+1955C>G	XP_011544138.1:n.427+1955C>G
XM_011545837.1:c.427+1955C>G	XP_011544139.1:n.427+1955C>G
XM_011545838.1:c.427+1955C>G	XP_011544140.1:n.427+1955C>G
XM_011545839.1:c.427+1955C>G	XP_011544141.1:n.427+1955C>G
XM_011545840.1:c.427+1955C>G	XP_011544142.1:n.427+1955C>G
XM_011545841.1:c.427+1955C>G	XP_011544143.1:n.427+1955C>G
XM_011545842.1:c.427+1955C>G	XP_011544144.1:n.427+1955C>G
XM_011545843.1:c.427+1955C>G	XP_011544145.1:n.427+1955C>G
XM_011545844.1:c.427+1955C>G	XP_011544146.1:n.427+1955C>G
XM_011545845.1:c.427+1955C>G	XP_011544147.1:n.427+1955C>G
XM_011545846.1:c.427+1955C>G	XP_011544148.1:n.427+1955C>G
XM_011545847.1:c.427+1955C>G	XP_011544149.1:n.427+1955C>G
XM_011545848.1:c.427+1955C>G	XP_011544150.1:n.427+1955C>G
XR_950791.1:n.543+1955C>G
NM_001318185.1:c.427+1955C>G	NP_001305114.1:n.427+1955C>G
XM_011545835.3:c.427+1955C>G	XP_011544137.1:n.427+1955C>G
XM_011545836.3:c.427+1955C>G	XP_011544138.1:n.427+1955C>G
XM_011545837.2:c.427+1955C>G	XP_011544139.1:n.427+1955C>G
XM_011545838.2:c.427+1955C>G	XP_011544140.1:n.427+1955C>G
XM_011545839.2:c.427+1955C>G	XP_011544141.1:n.427+1955C>G
XM_011545841.2:c.427+1955C>G	XP_011544143.1:n.427+1955C>G
XM_011545842.3:c.427+1955C>G	XP_011544144.1:n.427+1955C>G
XM_011545843.3:c.427+1955C>G	XP_011544145.1:n.427+1955C>G
XM_011545844.3:c.427+1955C>G	XP_011544146.1:n.427+1955C>G
XM_011545845.3:c.427+1955C>G	XP_011544147.1:n.427+1955C>G
XM_011545846.3:c.427+1955C>G	XP_011544148.1:n.427+1955C>G
XM_011545847.3:c.427+1955C>G	XP_011544149.1:n.427+1955C>G
XM_011545848.3:c.427+1955C>G	XP_011544150.1:n.427+1955C>G
XM_017023215.2:c.427+1955C>G	XP_016878704.1:n.427+1955C>G
XR_950791.2:n.555+1955C>G
NM_001318185.2:c.427+1955C>G	NP_001305114.1:n.427+1955C>G
NM_005353.3:c.427+1955C>G MANE Select	NP_005344.2:n.427+1955C>G