Canonical Allele Identifier: CA11183307

Gene: CRIM1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.36446412T>G , CM000664.2:g.36446412T>G	GRCh38
NC_000002.11:g.36673555T>G , CM000664.1:g.36673555T>G	GRCh37
NC_000002.10:g.36527059T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280527.7:c.869+3677T>G MANE Select	ENSP00000280527.2:n.869+3677T>G
ENST00000280527.6:c.869+3677T>G	ENSP00000280527.2:n.869+3677T>G
ENST00000426856.1:c.545+3677T>G	ENSP00000407636.1:n.545+3677T>G
NM_016441.2:c.869+3677T>G	NP_057525.1:n.869+3677T>G
XM_005264357.3:c.695+3677T>G	XP_005264414.1:n.695+3677T>G
XM_011532898.1:c.992+3677T>G	XP_011531200.1:n.992+3677T>G
XM_011532899.1:c.992+3677T>G	XP_011531201.1:n.992+3677T>G
XM_011532900.1:c.776+3677T>G	XP_011531202.1:n.776+3677T>G
XM_011532901.1:c.992+3677T>G	XP_011531203.1:n.992+3677T>G
XR_939687.1:n.1514+3677T>G
XM_005264357.5:c.695+3677T>G	XP_005264414.1:n.695+3677T>G
XM_011532898.3:c.992+3677T>G	XP_011531200.1:n.992+3677T>G
XM_011532899.3:c.992+3677T>G	XP_011531201.1:n.992+3677T>G
XM_011532901.3:c.992+3677T>G	XP_011531203.1:n.992+3677T>G
XM_017004258.2:c.749+3677T>G	XP_016859747.1:n.749+3677T>G
XM_017004259.1:c.869+3677T>G	XP_016859748.1:n.869+3677T>G
XM_017004260.2:c.626+3677T>G	XP_016859749.1:n.626+3677T>G
XM_017004261.1:c.25+3677T>G	XP_016859750.1:n.25+3677T>G
XM_017004262.1:c.25+3677T>G	XP_016859751.1:n.25+3677T>G
XM_024452945.1:c.395+3677T>G	XP_024308713.1:n.395+3677T>G
XM_024452946.1:c.395+3677T>G	XP_024308714.1:n.395+3677T>G
XM_024452947.1:c.395+3677T>G	XP_024308715.1:n.395+3677T>G
XM_024452948.1:c.395+3677T>G	XP_024308716.1:n.395+3677T>G
XR_001738763.2:n.1057+3677T>G
NM_016441.3:c.869+3677T>G MANE Select	NP_057525.1:n.869+3677T>G