Canonical Allele Identifier: CA12235745

Gene: CD2AP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.47585184T>A , CM000668.2:g.47585184T>A	GRCh38
NC_000006.11:g.47552920T>A , CM000668.1:g.47552920T>A	GRCh37
NC_000006.10:g.47660879T>A	NCBI36
NG_008878.1:g.112396T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359314.5:c.1108+3119T>A MANE Select	ENSP00000352264.5:n.1108+3119T>A
NM_012120.2:c.1108+3119T>A	NP_036252.1:n.1108+3119T>A
XM_005248976.1:c.1096+3119T>A	XP_005249033.1:n.1096+3119T>A
XM_005248977.2:c.1108+3119T>A	XP_005249034.1:n.1108+3119T>A
XM_011514449.1:c.961+3119T>A	XP_011512751.1:n.961+3119T>A
XM_011514449.2:c.961+3119T>A	XP_011512751.1:n.961+3119T>A
XM_017010641.1:c.1108+3119T>A	XP_016866130.1:n.1108+3119T>A
NM_012120.3:c.1108+3119T>A MANE Select	NP_036252.1:n.1108+3119T>A