Canonical Allele Identifier: CA2216992418

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265633_31265635delinsGTC , CM000678.2:g.31265633_31265635delinsGTC	GRCh38
NC_000016.9:g.31276954_31276956delinsGTC , CM000678.1:g.31276954_31276956delinsGTC	GRCh37
NC_000016.8:g.31184455_31184457delinsGTC	NCBI36
NG_011719.1:g.10667_10669delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.238+135_238+137delinsGTC MANE Select	ENSP00000441691.3:n.238+135_238+137delinsGTC
ENST00000648685.1:c.238+135_238+137delinsGTC	ENSP00000496959.1:n.238+135_238+137delinsGTC
ENST00000287497.12:c.238+135_238+137delinsGTC	ENSP00000287497.8:n.238+135_238+137delinsGTC
ENST00000544665.7:c.238+135_238+137delinsGTC	ENSP00000441691.2:n.238+135_238+137delinsGTC
NM_000632.3:c.238+135_238+137delinsGTC	NP_000623.2:n.238+135_238+137delinsGTC
NM_001145808.1:c.238+135_238+137delinsGTC	NP_001139280.1:n.238+135_238+137delinsGTC
XM_006721045.1:c.238+135_238+137delinsGTC	XP_006721108.1:n.238+135_238+137delinsGTC
XM_011545850.1:c.23+135_23+137delinsGTC	XP_011544152.1:n.23+135_23+137delinsGTC
XM_011545851.1:c.238+135_238+137delinsGTC	XP_011544153.1:n.238+135_238+137delinsGTC
XR_950796.1:n.328+135_328+137delinsGTC
XM_011545850.2:c.23+135_23+137delinsGTC	XP_011544152.1:n.23+135_23+137delinsGTC
XM_011545851.2:c.238+135_238+137delinsGTC	XP_011544153.1:n.238+135_238+137delinsGTC
XM_017023216.1:c.238+135_238+137delinsGTC	XP_016878705.1:n.238+135_238+137delinsGTC
NM_000632.4:c.238+135_238+137delinsGTC MANE Select	NP_000623.2:n.238+135_238+137delinsGTC
NM_001145808.2:c.238+135_238+137delinsGTC	NP_001139280.1:n.238+135_238+137delinsGTC