Canonical Allele Identifier: CA1282864038

Gene: MARCO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118967814_118967815delinsCT , CM000664.2:g.118967814_118967815delinsCT	GRCh38
NC_000002.11:g.119725390_119725391delinsCT , CM000664.1:g.119725390_119725391delinsCT	GRCh37
NC_000002.10:g.119441860_119441861delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327097.5:c.98-1346_98-1345delinsCT MANE Select	ENSP00000318916.4:n.98-1346_98-1345delinsCT
ENST00000327097.4:c.98-1346_98-1345delinsCT	ENSP00000318916.4:n.98-1346_98-1345delinsCT
ENST00000412481.1:c.-137-1346_-137-1345delinsCT	ENSP00000409192.1:n.-137-1346_-137-1345delinsCT
NM_006770.3:c.98-1346_98-1345delinsCT	NP_006761.1:n.98-1346_98-1345delinsCT
XM_011512082.1:c.98-1346_98-1345delinsCT	XP_011510384.1:n.98-1346_98-1345delinsCT
XM_011512083.1:c.98-6519_98-6518delinsCT	XP_011510385.1:n.98-6519_98-6518delinsCT
XM_011512082.2:c.98-1346_98-1345delinsCT	XP_011510384.1:n.98-1346_98-1345delinsCT
XM_011512083.3:c.98-6519_98-6518delinsCT	XP_011510385.1:n.98-6519_98-6518delinsCT
XM_017005171.2:c.98-1346_98-1345delinsCT	XP_016860660.1:n.98-1346_98-1345delinsCT
NM_006770.4:c.98-1346_98-1345delinsCT MANE Select	NP_006761.1:n.98-1346_98-1345delinsCT