Canonical Allele Identifier: CA719963231

Gene: ITGAM

Linked Data

• dbSNP Id: rs1331862152
• MyVariant Identifiers: chr16:g.31276955_31276956del (hg19) ; chr16:g.31265634_31265635del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265637_31265638del , CM000678.2:g.31265637_31265638del	GRCh38
NC_000016.9:g.31276958_31276959del , CM000678.1:g.31276958_31276959del	GRCh37
NC_000016.8:g.31184459_31184460del	NCBI36
NG_011719.1:g.10671_10672del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.238+139_238+140del MANE Select	ENSP00000441691.3:n.238+139_238+140del
ENST00000648685.1:c.238+139_238+140del	ENSP00000496959.1:n.238+139_238+140del
ENST00000287497.12:c.238+139_238+140del	ENSP00000287497.8:n.238+139_238+140del
ENST00000544665.7:c.238+139_238+140del	ENSP00000441691.2:n.238+139_238+140del
NM_000632.3:c.238+139_238+140del	NP_000623.2:n.238+139_238+140del
NM_001145808.1:c.238+139_238+140del	NP_001139280.1:n.238+139_238+140del
XM_006721045.1:c.238+139_238+140del	XP_006721108.1:n.238+139_238+140del
XM_011545850.1:c.23+139_23+140del	XP_011544152.1:n.23+139_23+140del
XM_011545851.1:c.238+139_238+140del	XP_011544153.1:n.238+139_238+140del
XR_950796.1:n.328+139_328+140del
XM_011545850.2:c.23+139_23+140del	XP_011544152.1:n.23+139_23+140del
XM_011545851.2:c.238+139_238+140del	XP_011544153.1:n.238+139_238+140del
XM_017023216.1:c.238+139_238+140del	XP_016878705.1:n.238+139_238+140del
NM_000632.4:c.238+139_238+140del MANE Select	NP_000623.2:n.238+139_238+140del
NM_001145808.2:c.238+139_238+140del	NP_001139280.1:n.238+139_238+140del