Canonical Allele Identifier: CA2360158867

Gene: TM9SF4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32137845A>T , CM000682.2:g.32137845A>T	GRCh38
NC_000020.10:g.30725648A>T , CM000682.1:g.30725648A>T	GRCh37
NC_000020.9:g.30189309A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398022.7:c.229+1672A>T MANE Select	ENSP00000381104.2:n.229+1672A>T
ENST00000217315.9:c.178+1672A>T	ENSP00000217315.5:n.178+1672A>T
ENST00000398022.6:c.229+1672A>T	ENSP00000381104.2:n.229+1672A>T
ENST00000417389.1:c.178+1672A>T	ENSP00000404755.1:n.178+1672A>T
ENST00000442842.5:c.*92+848A>T	ENSP00000413382.1:n.*92+848A>T
ENST00000450829.5:c.*92+848A>T	ENSP00000390314.1:n.*92+848A>T
NM_014742.3:c.229+1672A>T	NP_055557.2:n.229+1672A>T
XM_005260622.3:c.178+1672A>T	XP_005260679.1:n.178+1672A>T
NM_001363731.1:c.178+1672A>T	NP_001350660.1:n.178+1672A>T
XM_017028154.1:c.229+1672A>T	XP_016883643.1:n.229+1672A>T
XM_017028155.1:c.178+1672A>T	XP_016883644.1:n.178+1672A>T
XM_017028156.1:c.-7+1672A>T	XP_016883645.1:n.-7+1672A>T
XM_017028157.1:c.-7+1672A>T	XP_016883646.1:n.-7+1672A>T
XM_017028158.1:c.-7+1672A>T	XP_016883647.1:n.-7+1672A>T
XM_017028159.1:c.-560+1672A>T	XP_016883648.1:n.-560+1672A>T
XM_017028160.1:c.-516+1672A>T	XP_016883649.1:n.-516+1672A>T
XM_017028161.1:c.-560+1672A>T	XP_016883650.1:n.-560+1672A>T
NM_014742.4:c.229+1672A>T MANE Select	NP_055557.2:n.229+1672A>T
NM_001363731.2:c.178+1672A>T	NP_001350660.1:n.178+1672A>T