Canonical Allele Identifier: CA906249951

Gene: CMTM8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32288005C>G , CM000665.2:g.32288005C>G	GRCh38
NC_000003.11:g.32329497C>G , CM000665.1:g.32329497C>G	GRCh37
NC_000003.10:g.32304501C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307526.4:c.147+48886C>G MANE Select	ENSP00000307741.3:n.147+48886C>G
ENST00000307526.3:c.147+48886C>G	ENSP00000307741.3:n.147+48886C>G
ENST00000458535.6:c.147+48886C>G	ENSP00000412934.2:n.147+48886C>G
NM_178868.3:c.147+48886C>G	NP_849199.2:n.147+48886C>G
XM_011533416.1:c.216+5346C>G	XP_011531718.1:n.216+5346C>G
XM_011533417.1:c.147+48886C>G	XP_011531719.1:n.147+48886C>G
NM_001320308.1:c.147+48886C>G	NP_001307237.1:n.147+48886C>G
NM_178868.4:c.147+48886C>G	NP_849199.2:n.147+48886C>G
XM_011533416.3:c.216+5346C>G	XP_011531718.1:n.216+5346C>G
NM_178868.5:c.147+48886C>G MANE Select	NP_849199.2:n.147+48886C>G
NM_001320308.2:c.147+48886C>G	NP_001307237.1:n.147+48886C>G