Canonical Allele Identifier: CA415385318

Gene: ATAD3A

Linked Data

• gnomAD v4: 1-1512331-T-C
• MyVariant Identifiers: chr1:g.1447711T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512331T>C , CM000663.2:g.1512331T>C	GRCh38
NC_000001.10:g.1447711T>C , CM000663.1:g.1447711T>C	GRCh37
NC_000001.9:g.1437574T>C	NCBI36
NG_053035.1:g.5189T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378756.8:c.63T>C MANE Select	ENSP00000368031.3:p.Pro21=
ENST00000672388.1:n.167T>C
ENST00000378755.9:c.63T>C	ENSP00000368030.5:p.Pro21=
ENST00000378756.7:c.63T>C	ENSP00000368031.3:p.Pro21=
NM_001170535.1:c.63T>C	NP_001164006.1:p.Pro21=
NM_018188.3:c.63T>C	NP_060658.3:p.Pro21=
NM_001170535.2:c.63T>C	NP_001164006.1:p.Pro21=
NM_018188.4:c.63T>C	NP_060658.3:p.Pro21=
XM_024448098.1:c.63T>C	XP_024303866.1:p.Pro21=
XR_001737282.1:n.189T>C
XR_002956997.1:n.189T>C
NM_001170535.3:c.63T>C MANE Select	NP_001164006.1:p.Pro21=
NM_018188.5:c.63T>C	NP_060658.3:p.Pro21=