Canonical Allele Identifier: CA2668475168

Gene: MYNN

Linked Data

• gnomAD v4: 3-169784790-G-GTAAATCTCATCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784790_169784791insTAAATCTCATCTC , CM000665.2:g.169784790_169784791insTAAATCTCATCTC	GRCh38
NC_000003.11:g.169502578_169502579insTAAATCTCATCTC , CM000665.1:g.169502578_169502579insTAAATCTCATCTC	GRCh37
NC_000003.10:g.170985272_170985273insTAAATCTCATCTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+82_1570+83insTAAATCTCATCTC MANE Select	ENSP00000326240.4:n.1570+82_1570+83insTAAATCTCATCTC
ENST00000349841.9:c.1570+82_1570+83insTAAATCTCATCTC	ENSP00000326240.4:n.1570+82_1570+83insTAAATCTCATCTC
ENST00000356716.8:c.1570+82_1570+83insTAAATCTCATCTC	ENSP00000349150.3:n.1570+82_1570+83insTAAATCTCATCTC
ENST00000544106.5:c.1483+1230_1483+1231insTAAATCTCATCTC	ENSP00000440637.1:n.1483+1230_1483+1231insTAAATCTCATCTC
ENST00000602751.5:c.*1178+82_*1178+83insTAAATCTCATCTC	ENSP00000473654.1:n.*1178+82_*1178+83insTAAATCTCATCTC
NM_001185118.1:c.1570+82_1570+83insTAAATCTCATCTC	NP_001172047.1:n.1570+82_1570+83insTAAATCTCATCTC
NM_001185119.1:c.1483+1230_1483+1231insTAAATCTCATCTC	NP_001172048.1:n.1483+1230_1483+1231insTAAATCTCATCTC
NM_018657.4:c.1570+82_1570+83insTAAATCTCATCTC	NP_061127.1:n.1570+82_1570+83insTAAATCTCATCTC
NR_033702.1:n.1869+82_1869+83insTAAATCTCATCTC
NR_033703.1:n.1883+82_1883+83insTAAATCTCATCTC
XM_005247621.3:c.1486+82_1486+83insTAAATCTCATCTC	XP_005247678.1:n.1486+82_1486+83insTAAATCTCATCTC
XM_005247622.3:c.1324+82_1324+83insTAAATCTCATCTC	XP_005247679.1:n.1324+82_1324+83insTAAATCTCATCTC
XM_005247624.3:c.1228+82_1228+83insTAAATCTCATCTC	XP_005247681.1:n.1228+82_1228+83insTAAATCTCATCTC
XM_011512987.1:c.1570+82_1570+83insTAAATCTCATCTC	XP_011511289.1:n.1570+82_1570+83insTAAATCTCATCTC
XM_011512988.1:c.1570+82_1570+83insTAAATCTCATCTC	XP_011511290.1:n.1570+82_1570+83insTAAATCTCATCTC
XM_005247621.5:c.1486+82_1486+83insTAAATCTCATCTC	XP_005247678.1:n.1486+82_1486+83insTAAATCTCATCTC
XM_005247622.4:c.1324+82_1324+83insTAAATCTCATCTC	XP_005247679.1:n.1324+82_1324+83insTAAATCTCATCTC
XM_005247624.4:c.1228+82_1228+83insTAAATCTCATCTC	XP_005247681.1:n.1228+82_1228+83insTAAATCTCATCTC
XM_017006864.2:c.1570+82_1570+83insTAAATCTCATCTC	XP_016862353.1:n.1570+82_1570+83insTAAATCTCATCTC
XM_017006865.2:c.1144+82_1144+83insTAAATCTCATCTC	XP_016862354.1:n.1144+82_1144+83insTAAATCTCATCTC
XM_017006866.2:c.1144+82_1144+83insTAAATCTCATCTC	XP_016862355.1:n.1144+82_1144+83insTAAATCTCATCTC
XM_017006867.2:c.751+82_751+83insTAAATCTCATCTC	XP_016862356.1:n.751+82_751+83insTAAATCTCATCTC
XM_017006868.2:c.667+82_667+83insTAAATCTCATCTC	XP_016862357.1:n.667+82_667+83insTAAATCTCATCTC
XR_002959552.1:n.3402+82_3402+83insTAAATCTCATCTC
NM_001185118.2:c.1570+82_1570+83insTAAATCTCATCTC	NP_001172047.1:n.1570+82_1570+83insTAAATCTCATCTC
NM_018657.5:c.1570+82_1570+83insTAAATCTCATCTC MANE Select	NP_061127.1:n.1570+82_1570+83insTAAATCTCATCTC
NR_033702.2:n.1538+82_1538+83insTAAATCTCATCTC
NR_033703.2:n.1552+82_1552+83insTAAATCTCATCTC