Canonical Allele Identifier: CA755826829

Gene: MARCO

Linked Data

• dbSNP Id: rs1463288204
• gnomAD v3: 2-118967692-AGGGGTCCCTGCTGTGCG-A
• gnomAD v4: 2-118967692-AGGGGTCCCTGCTGTGCG-A
• MyVariant Identifiers: chr2:g.119725269_119725285del (hg19) ; chr2:g.118967693_118967709del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118967698_118967714del , CM000664.2:g.118967698_118967714del	GRCh38
NC_000002.11:g.119725274_119725290del , CM000664.1:g.119725274_119725290del	GRCh37
NC_000002.10:g.119441744_119441760del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327097.5:c.98-1462_98-1446del MANE Select	ENSP00000318916.4:n.98-1462_98-1446del
ENST00000327097.4:c.98-1462_98-1446del	ENSP00000318916.4:n.98-1462_98-1446del
ENST00000412481.1:c.-137-1462_-137-1446del	ENSP00000409192.1:n.-137-1462_-137-1446del
NM_006770.3:c.98-1462_98-1446del	NP_006761.1:n.98-1462_98-1446del
XM_011512082.1:c.98-1462_98-1446del	XP_011510384.1:n.98-1462_98-1446del
XM_011512083.1:c.98-6635_98-6619del	XP_011510385.1:n.98-6635_98-6619del
XM_011512082.2:c.98-1462_98-1446del	XP_011510384.1:n.98-1462_98-1446del
XM_011512083.3:c.98-6635_98-6619del	XP_011510385.1:n.98-6635_98-6619del
XM_017005171.2:c.98-1462_98-1446del	XP_016860660.1:n.98-1462_98-1446del
NM_006770.4:c.98-1462_98-1446del MANE Select	NP_006761.1:n.98-1462_98-1446del