Canonical Allele Identifier: CA284127339

Gene: MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79598609_79598610del , CM000678.2:g.79598609_79598610del	GRCh38
NC_000016.9:g.79632506_79632507del , CM000678.1:g.79632506_79632507del	GRCh37
NC_000016.8:g.78190007_78190008del	NCBI36
NG_016440.1:g.7143_7144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326043.5:c.1118+202_1118+203del MANE Select	ENSP00000327048.4:n.1118+202_1118+203del
ENST00000326043.4:c.1118+202_1118+203del	ENSP00000327048.4:n.1118+202_1118+203del
ENST00000393350.1:c.*198_*199del	ENSP00000377019.1:n.*198_*199del
ENST00000569649.1:c.1118+202_1118+203del	ENSP00000455097.1:n.1118+202_1118+203del
NM_001031804.2:c.*198_*199del	NP_001026974.1:n.*198_*199del
NM_005360.4:c.1118+202_1118+203del	NP_005351.2:n.1118+202_1118+203del
XM_011523084.1:c.1118+202_1118+203del	XP_011521386.1:n.1118+202_1118+203del
XM_017023233.2:c.1118+202_1118+203del	XP_016878722.1:n.1118+202_1118+203del
XM_017023234.2:c.1118+202_1118+203del	XP_016878723.1:n.1118+202_1118+203del
XM_017023235.2:c.1118+202_1118+203del	XP_016878724.1:n.1118+202_1118+203del
XM_024450279.1:c.1118+202_1118+203del	XP_024306047.1:n.1118+202_1118+203del
XR_001751902.2:n.3168+202_3168+203del
XR_002957802.1:n.3168+202_3168+203del
XR_002957803.1:n.3168+202_3168+203del
XR_002957804.1:n.3168+202_3168+203del
NM_005360.5:c.1118+202_1118+203del MANE Select	NP_005351.2:n.1118+202_1118+203del
NM_001031804.3:c.*198_*199del	NP_001026974.1:n.*198_*199del