Canonical Allele Identifier: CA1282864133

Gene: MARCO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118968042_118968044delinsCTG , CM000664.2:g.118968042_118968044delinsCTG	GRCh38
NC_000002.11:g.119725618_119725620delinsCTG , CM000664.1:g.119725618_119725620delinsCTG	GRCh37
NC_000002.10:g.119442088_119442090delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327097.5:c.98-1118_98-1116delinsCTG MANE Select	ENSP00000318916.4:n.98-1118_98-1116delinsCTG
ENST00000327097.4:c.98-1118_98-1116delinsCTG	ENSP00000318916.4:n.98-1118_98-1116delinsCTG
ENST00000412481.1:c.-137-1118_-137-1116delinsCTG	ENSP00000409192.1:n.-137-1118_-137-1116delinsCTG
NM_006770.3:c.98-1118_98-1116delinsCTG	NP_006761.1:n.98-1118_98-1116delinsCTG
XM_011512082.1:c.98-1118_98-1116delinsCTG	XP_011510384.1:n.98-1118_98-1116delinsCTG
XM_011512083.1:c.98-6291_98-6289delinsCTG	XP_011510385.1:n.98-6291_98-6289delinsCTG
XM_011512082.2:c.98-1118_98-1116delinsCTG	XP_011510384.1:n.98-1118_98-1116delinsCTG
XM_011512083.3:c.98-6291_98-6289delinsCTG	XP_011510385.1:n.98-6291_98-6289delinsCTG
XM_017005171.2:c.98-1118_98-1116delinsCTG	XP_016860660.1:n.98-1118_98-1116delinsCTG
NM_006770.4:c.98-1118_98-1116delinsCTG MANE Select	NP_006761.1:n.98-1118_98-1116delinsCTG