Canonical Allele Identifier: CA16099014

Gene: CCDC85A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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