Canonical Allele Identifier: CA14405797

Gene: MYCBPAP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50513848A>G , CM000679.2:g.50513848A>G	GRCh38
NC_000017.10:g.48591209A>G , CM000679.1:g.48591209A>G	GRCh37
NC_000017.9:g.45946208A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452039.7:c.77-2722A>G	ENSP00000407145.3:n.77-2722A>G
ENST00000323776.11:c.77-2722A>G MANE Select	ENSP00000323184.6:n.77-2722A>G
ENST00000437498.2:c.77-2722A>G	ENSP00000414583.2:n.77-2722A>G
ENST00000452039.6:c.77-2722A>G	ENSP00000407145.2:n.77-2722A>G
ENST00000458692.2:c.77-997A>G	ENSP00000397686.2:n.77-997A>G
ENST00000652471.1:c.206-2722A>G	ENSP00000498665.1:n.206-2722A>G
ENST00000323776.9:c.206-2722A>G	ENSP00000323184.5:n.206-2722A>G
ENST00000436259.6:c.95-2722A>G	ENSP00000397209.2:n.95-2722A>G
ENST00000437498.1:c.130-2722A>G
ENST00000452039.5:c.206-2722A>G	ENSP00000407145.1:n.206-2722A>G
ENST00000458692.1:c.164-997A>G
ENST00000470609.5:n.327-2722A>G
ENST00000576179.1:n.303-2011A>G
NM_032133.4:c.206-2722A>G	NP_115509.4:n.206-2722A>G
XM_005257725.2:c.206-2722A>G	XP_005257782.1:n.206-2722A>G
XM_005257726.2:c.206-2722A>G	XP_005257783.1:n.206-2722A>G
XM_011525342.1:c.206-2722A>G	XP_011523644.1:n.206-2722A>G
XM_011525343.1:c.206-2722A>G	XP_011523645.1:n.206-2722A>G
XR_934571.1:n.211-2722A>G
XR_934572.1:n.211-2722A>G
XR_934573.1:n.211-2722A>G
XR_934574.1:n.211-2722A>G
NM_001366294.1:c.77-2722A>G	NP_001353223.1:n.77-2722A>G
NM_032133.5:c.77-2722A>G	NP_115509.5:n.77-2722A>G
NR_158785.1:n.313-2722A>G
XM_017025205.1:c.206-2722A>G	XP_016880694.1:n.206-2722A>G
XR_001752658.1:n.211-2722A>G
XR_001752659.1:n.324-2722A>G
XR_002958075.1:n.211-2722A>G
NM_001366294.2:c.77-2722A>G	NP_001353223.1:n.77-2722A>G
NM_032133.6:c.77-2722A>G MANE Select	NP_115509.5:n.77-2722A>G
NR_158785.2:n.313-2722A>G