Canonical Allele Identifier: CA1252746155
Gene: CCDC85A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.56354428C= , CM000664.2:g.56354428C= GRCh38
NC_000002.11:g.56581563C= , CM000664.1:g.56581563C= GRCh37
NC_000002.10:g.56435067C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000407595.3:c.1317+11473C= MANE Select ENSP00000384040.2:n.1317+11473C=
ENST00000407595.2:c.1317+11473C= ENSP00000384040.2:n.1317+11473C=
NM_001080433.1:c.1317+11473C= NP_001073902.1:n.1317+11473C=
XM_005264125.1:c.1317+11473C= XP_005264182.1:n.1317+11473C=
NM_001348512.1:c.1317+11473C= NP_001335441.1:n.1317+11473C=
NM_001348513.1:c.1317+11473C= NP_001335442.1:n.1317+11473C=
NM_001348514.1:c.1317+11473C= NP_001335443.1:n.1317+11473C=
NM_001348515.1:c.1317+11473C= NP_001335444.1:n.1317+11473C=
NM_001348516.1:c.1241-29838C= NP_001335445.1:n.1241-29838C=
XM_024452642.1:c.1230+11473C= XP_024308410.1:n.1230+11473C=
NM_001080433.2:c.1317+11473C= MANE Select NP_001073902.1:n.1317+11473C=