Canonical Allele Identifier: CA505476137

Gene: ICAM3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10338716A>C , CM000681.2:g.10338716A>C	GRCh38
NC_000019.9:g.10449392A>C , CM000681.1:g.10449392A>C	GRCh37
NC_000019.8:g.10310392A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000160262.10:c.309T>G MANE Select	ENSP00000160262.3:p.Ser103=
ENST00000160262.9:c.309T>G	ENSP00000160262.3:p.Ser103=
ENST00000585439.1:c.*44T>G	ENSP00000466501.1:n.*44T>G
ENST00000587992.1:n.356T>G
ENST00000589249.1:c.78T>G	ENSP00000466081.1:p.Ser26=
ENST00000589261.5:c.78T>G	ENSP00000468333.1:p.Ser26=
ENST00000589900.5:n.324T>G
ENST00000590569.1:c.276T>G	ENSP00000467770.1:p.Ser92=
NM_002162.3:c.309T>G	NP_002153.2:p.Ser103=
XM_011527959.1:c.78T>G	XP_011526261.1:p.Ser26=
XM_011527960.1:c.309T>G	XP_011526262.1:p.Ser103=
NM_001320605.1:c.309T>G	NP_001307534.1:p.Ser103=
NM_001320606.1:c.78T>G	NP_001307535.1:p.Ser26=
NM_001320608.1:c.-792T>G	NP_001307537.1:n.-792T>G
NM_002162.4:c.309T>G	NP_002153.2:p.Ser103=
NM_002162.5:c.309T>G MANE Select	NP_002153.2:p.Ser103=
NM_001320605.2:c.309T>G	NP_001307534.1:p.Ser103=
NM_001320606.2:c.78T>G	NP_001307535.1:p.Ser26=
NM_001320608.2:c.-792T>G	NP_001307537.1:n.-792T>G