Canonical Allele Identifier: CA395682728

Gene: ITGAM

Linked Data

• MyVariant Identifiers: chr16:g.31265431_31265445del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265432_31265446del , CM000678.2:g.31265432_31265446del	GRCh38
NC_000016.9:g.31276753_31276767del , CM000678.1:g.31276753_31276767del	GRCh37
NC_000016.8:g.31184254_31184268del	NCBI36
NG_011719.1:g.10466_10480del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.172_186del MANE Select	ENSP00000441691.3:p.Asn58_Ser62del
ENST00000648685.1:c.172_186del	ENSP00000496959.1:p.Asn58_Ser62del
ENST00000287497.12:c.172_186del	ENSP00000287497.8:p.Asn58_Ser62del
ENST00000544665.7:c.172_186del	ENSP00000441691.2:p.Asn58_Ser62del
NM_000632.3:c.172_186del	NP_000623.2:p.Asn58_Ser62del
NM_001145808.1:c.172_186del	NP_001139280.1:p.Asn58_Ser62del
XM_006721045.1:c.172_186del	XP_006721108.1:p.Asn58_Ser62del
XM_011545850.1:c.-44_-30del	XP_011544152.1:n.-44_-30del
XM_011545851.1:c.172_186del	XP_011544153.1:p.Asn58_Ser62del
XR_950796.1:n.262_276del
XM_011545850.2:c.-44_-30del	XP_011544152.1:n.-44_-30del
XM_011545851.2:c.172_186del	XP_011544153.1:p.Asn58_Ser62del
XM_017023216.1:c.172_186del	XP_016878705.1:p.Asn58_Ser62del
NM_000632.4:c.172_186del MANE Select	NP_000623.2:p.Asn58_Ser62del
NM_001145808.2:c.172_186del	NP_001139280.1:p.Asn58_Ser62del