Canonical Allele Identifier: CA2668475219

Gene: MYNN

Linked Data

• gnomAD v4: 3-169784824-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784825_169784826insAA , CM000665.2:g.169784825_169784826insAA	GRCh38
NC_000003.11:g.169502613_169502614insAA , CM000665.1:g.169502613_169502614insAA	GRCh37
NC_000003.10:g.170985307_170985308insAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+117_1570+118insAA MANE Select	ENSP00000326240.4:n.1570+117_1570+118insAA
ENST00000349841.9:c.1570+117_1570+118insAA	ENSP00000326240.4:n.1570+117_1570+118insAA
ENST00000356716.8:c.1570+117_1570+118insAA	ENSP00000349150.3:n.1570+117_1570+118insAA
ENST00000544106.5:c.1483+1265_1483+1266insAA	ENSP00000440637.1:n.1483+1265_1483+1266insAA
ENST00000602751.5:c.*1178+117_*1178+118insAA	ENSP00000473654.1:n.*1178+117_*1178+118insAA
NM_001185118.1:c.1570+117_1570+118insAA	NP_001172047.1:n.1570+117_1570+118insAA
NM_001185119.1:c.1483+1265_1483+1266insAA	NP_001172048.1:n.1483+1265_1483+1266insAA
NM_018657.4:c.1570+117_1570+118insAA	NP_061127.1:n.1570+117_1570+118insAA
NR_033702.1:n.1869+117_1869+118insAA
NR_033703.1:n.1883+117_1883+118insAA
XM_005247621.3:c.1486+117_1486+118insAA	XP_005247678.1:n.1486+117_1486+118insAA
XM_005247622.3:c.1324+117_1324+118insAA	XP_005247679.1:n.1324+117_1324+118insAA
XM_005247624.3:c.1228+117_1228+118insAA	XP_005247681.1:n.1228+117_1228+118insAA
XM_011512987.1:c.1570+117_1570+118insAA	XP_011511289.1:n.1570+117_1570+118insAA
XM_011512988.1:c.1570+117_1570+118insAA	XP_011511290.1:n.1570+117_1570+118insAA
XM_005247621.5:c.1486+117_1486+118insAA	XP_005247678.1:n.1486+117_1486+118insAA
XM_005247622.4:c.1324+117_1324+118insAA	XP_005247679.1:n.1324+117_1324+118insAA
XM_005247624.4:c.1228+117_1228+118insAA	XP_005247681.1:n.1228+117_1228+118insAA
XM_017006864.2:c.1570+117_1570+118insAA	XP_016862353.1:n.1570+117_1570+118insAA
XM_017006865.2:c.1144+117_1144+118insAA	XP_016862354.1:n.1144+117_1144+118insAA
XM_017006866.2:c.1144+117_1144+118insAA	XP_016862355.1:n.1144+117_1144+118insAA
XM_017006867.2:c.751+117_751+118insAA	XP_016862356.1:n.751+117_751+118insAA
XM_017006868.2:c.667+117_667+118insAA	XP_016862357.1:n.667+117_667+118insAA
XR_002959552.1:n.3402+117_3402+118insAA
NM_001185118.2:c.1570+117_1570+118insAA	NP_001172047.1:n.1570+117_1570+118insAA
NM_018657.5:c.1570+117_1570+118insAA MANE Select	NP_061127.1:n.1570+117_1570+118insAA
NR_033702.2:n.1538+117_1538+118insAA
NR_033703.2:n.1552+117_1552+118insAA