Canonical Allele Identifier: CA1282864200
Gene: MARCO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118968181_118968182delinsTC , CM000664.2:g.118968181_118968182delinsTC GRCh38
NC_000002.11:g.119725757_119725758delinsTC , CM000664.1:g.119725757_119725758delinsTC GRCh37
NC_000002.10:g.119442227_119442228delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327097.5:c.98-979_98-978delinsTC MANE Select ENSP00000318916.4:n.98-979_98-978delinsTC
ENST00000327097.4:c.98-979_98-978delinsTC ENSP00000318916.4:n.98-979_98-978delinsTC
ENST00000412481.1:c.-137-979_-137-978delinsTC ENSP00000409192.1:n.-137-979_-137-978delinsTC
NM_006770.3:c.98-979_98-978delinsTC NP_006761.1:n.98-979_98-978delinsTC
XM_011512082.1:c.98-979_98-978delinsTC XP_011510384.1:n.98-979_98-978delinsTC
XM_011512083.1:c.98-6152_98-6151delinsTC XP_011510385.1:n.98-6152_98-6151delinsTC
XM_011512082.2:c.98-979_98-978delinsTC XP_011510384.1:n.98-979_98-978delinsTC
XM_011512083.3:c.98-6152_98-6151delinsTC XP_011510385.1:n.98-6152_98-6151delinsTC
XM_017005171.2:c.98-979_98-978delinsTC XP_016860660.1:n.98-979_98-978delinsTC
NM_006770.4:c.98-979_98-978delinsTC MANE Select NP_006761.1:n.98-979_98-978delinsTC