Canonical Allele Identifier: CA1282864213
Gene: MARCO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118968203_118968204delinsGA , CM000664.2:g.118968203_118968204delinsGA GRCh38
NC_000002.11:g.119725779_119725780delinsGA , CM000664.1:g.119725779_119725780delinsGA GRCh37
NC_000002.10:g.119442249_119442250delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327097.5:c.98-957_98-956delinsGA MANE Select ENSP00000318916.4:n.98-957_98-956delinsGA
ENST00000327097.4:c.98-957_98-956delinsGA ENSP00000318916.4:n.98-957_98-956delinsGA
ENST00000412481.1:c.-137-957_-137-956delinsGA ENSP00000409192.1:n.-137-957_-137-956delinsGA
NM_006770.3:c.98-957_98-956delinsGA NP_006761.1:n.98-957_98-956delinsGA
XM_011512082.1:c.98-957_98-956delinsGA XP_011510384.1:n.98-957_98-956delinsGA
XM_011512083.1:c.98-6130_98-6129delinsGA XP_011510385.1:n.98-6130_98-6129delinsGA
XM_011512082.2:c.98-957_98-956delinsGA XP_011510384.1:n.98-957_98-956delinsGA
XM_011512083.3:c.98-6130_98-6129delinsGA XP_011510385.1:n.98-6130_98-6129delinsGA
XM_017005171.2:c.98-957_98-956delinsGA XP_016860660.1:n.98-957_98-956delinsGA
NM_006770.4:c.98-957_98-956delinsGA MANE Select NP_006761.1:n.98-957_98-956delinsGA