Canonical Allele Identifier: CA395681057

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31321334C>A , CM000678.2:g.31321334C>A	GRCh38
NC_000016.9:g.31332655C>A , CM000678.1:g.31332655C>A	GRCh37
NC_000016.8:g.31240156C>A	NCBI36
NG_011719.1:g.66368C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000632.4:c.1801C>A MANE Select	NP_000623.2:p.Leu601Met
ENST00000544665.9:c.1801C>A MANE Select	ENSP00000441691.3:p.Leu601Met
NM_000632.3:c.1801C>A	NP_000623.2:p.Leu601Met
NM_001145808.1:c.1804C>A	NP_001139280.1:p.Leu602Met
NM_001145808.2:c.1804C>A	NP_001139280.1:p.Leu602Met
ENST00000287497.12:c.1801C>A	ENSP00000287497.8:p.Leu601Met
ENST00000544665.7:c.1804C>A	ENSP00000441691.2:p.Leu602Met
ENST00000567031.1:c.454-3065C>A
ENST00000648685.1:c.1804C>A	ENSP00000496959.1:p.Leu602Met
XM_006721045.1:c.1801C>A	XP_006721108.1:p.Leu601Met
XM_011545850.1:c.1618C>A	XP_011544152.1:p.Leu540Met
XM_011545850.2:c.1618C>A	XP_011544152.1:p.Leu540Met
XM_011545851.1:c.1804C>A	XP_011544153.1:p.Leu602Met
XM_011545851.2:c.1804C>A	XP_011544153.1:p.Leu602Met
XM_017023216.1:c.1804C>A	XP_016878705.1:p.Leu602Met
XR_950796.1:n.1894C>A