Canonical Allele Identifier: CA415385310
Gene: ATAD3A HGNC NCBI

Linked Data

dbSNP Id: rs1175372911
MyVariant Identifiers: chr1:g.1447702G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512322G>C , CM000663.2:g.1512322G>C GRCh38
NC_000001.10:g.1447702G>C , CM000663.1:g.1447702G>C GRCh37
NC_000001.9:g.1437565G>C NCBI36
NG_053035.1:g.5180G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378756.8:c.54G>C MANE Select ENSP00000368031.3:p.Pro18=
ENST00000672388.1:n.158G>C
ENST00000378755.9:c.54G>C ENSP00000368030.5:p.Pro18=
ENST00000378756.7:c.54G>C ENSP00000368031.3:p.Pro18=
NM_001170535.1:c.54G>C NP_001164006.1:p.Pro18=
NM_018188.3:c.54G>C NP_060658.3:p.Pro18=
NM_001170535.2:c.54G>C NP_001164006.1:p.Pro18=
NM_018188.4:c.54G>C NP_060658.3:p.Pro18=
XM_024448098.1:c.54G>C XP_024303866.1:p.Pro18=
XR_001737282.1:n.180G>C
XR_002956997.1:n.180G>C
NM_001170535.3:c.54G>C MANE Select NP_001164006.1:p.Pro18=
NM_018188.5:c.54G>C NP_060658.3:p.Pro18=