Canonical Allele Identifier: CA2216992025

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265429_31265444delinsGCCAACCAAAGGGGCA , CM000678.2:g.31265429_31265444delinsGCCAACCAAAGGGGCA	GRCh38
NC_000016.9:g.31276750_31276765delinsGCCAACCAAAGGGGCA , CM000678.1:g.31276750_31276765delinsGCCAACCAAAGGGGCA	GRCh37
NC_000016.8:g.31184251_31184266delinsGCCAACCAAAGGGGCA	NCBI36
NG_011719.1:g.10463_10478delinsGCCAACCAAAGGGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.169_184delinsGCCAACCAAAGGGGCA MANE Select	ENSP00000441691.3:p.Ala57=
ENST00000648685.1:c.169_184delinsGCCAACCAAAGGGGCA	ENSP00000496959.1:p.Ala57=
ENST00000287497.12:c.169_184delinsGCCAACCAAAGGGGCA	ENSP00000287497.8:p.Ala57=
ENST00000544665.7:c.169_184delinsGCCAACCAAAGGGGCA	ENSP00000441691.2:p.Ala57=
NM_000632.3:c.169_184delinsGCCAACCAAAGGGGCA	NP_000623.2:p.Ala57=
NM_001145808.1:c.169_184delinsGCCAACCAAAGGGGCA	NP_001139280.1:p.Ala57=
XM_006721045.1:c.169_184delinsGCCAACCAAAGGGGCA	XP_006721108.1:p.Ala57=
XM_011545850.1:c.-47_-32delinsGCCAACCAAAGGGGCA	XP_011544152.1:n.-47_-32delinsGCCAACCAAAGGGGCA
XM_011545851.1:c.169_184delinsGCCAACCAAAGGGGCA	XP_011544153.1:p.Ala57=
XR_950796.1:n.259_274delinsGCCAACCAAAGGGGCA
XM_011545850.2:c.-47_-32delinsGCCAACCAAAGGGGCA	XP_011544152.1:n.-47_-32delinsGCCAACCAAAGGGGCA
XM_011545851.2:c.169_184delinsGCCAACCAAAGGGGCA	XP_011544153.1:p.Ala57=
XM_017023216.1:c.169_184delinsGCCAACCAAAGGGGCA	XP_016878705.1:p.Ala57=
NM_000632.4:c.169_184delinsGCCAACCAAAGGGGCA MANE Select	NP_000623.2:p.Ala57=
NM_001145808.2:c.169_184delinsGCCAACCAAAGGGGCA	NP_001139280.1:p.Ala57=