Canonical Allele Identifier: CA289312664

Gene: ATAD5

Linked Data

• dbSNP Id: rs3764419
• gnomAD v2: 17-29164023-C-G
• gnomAD v3: 17-30837005-C-G
• gnomAD v4: 17-30837005-C-G
• MyVariant Identifiers: chr17:g.29164023C>G (hg19) ; chr17:g.30837005C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30837005C>G , CM000679.2:g.30837005C>G	GRCh38
NC_000017.10:g.29164023C>G , CM000679.1:g.29164023C>G	GRCh37
NC_000017.9:g.26188149C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321990.5:c.1968-201C>G MANE Select	ENSP00000313171.4:n.1968-201C>G
ENST00000321990.4:c.1968-201C>G	ENSP00000313171.4:n.1968-201C>G
ENST00000578295.5:c.1968-201C>G	ENSP00000463102.1:n.1968-201C>G
ENST00000585133.1:n.841-201C>G
NM_024857.4:c.1968-201C>G	NP_079133.3:n.1968-201C>G
XM_011525269.1:c.1968-201C>G	XP_011523571.1:n.1968-201C>G
XM_011525270.1:c.1968-201C>G	XP_011523572.1:n.1968-201C>G
XM_011525271.1:c.1968-201C>G	XP_011523573.1:n.1968-201C>G
XM_011525272.1:c.1968-201C>G	XP_011523574.1:n.1968-201C>G
XM_011525273.1:c.1968-201C>G	XP_011523575.1:n.1968-201C>G
XR_934553.1:n.2575-201C>G
XM_011525269.3:c.1968-201C>G	XP_011523571.1:n.1968-201C>G
XM_011525270.3:c.1968-201C>G	XP_011523572.1:n.1968-201C>G
XM_011525273.3:c.1968-201C>G	XP_011523575.1:n.1968-201C>G
XR_001752631.2:n.3486-201C>G
XR_001752632.2:n.3486-201C>G
XR_934553.3:n.3486-201C>G
NM_024857.5:c.1968-201C>G MANE Select	NP_079133.3:n.1968-201C>G