Canonical Allele Identifier: CA2668475212

Gene: MYNN

Linked Data

• gnomAD v4: 3-169784818-GAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784819_169784820del , CM000665.2:g.169784819_169784820del	GRCh38
NC_000003.11:g.169502607_169502608del , CM000665.1:g.169502607_169502608del	GRCh37
NC_000003.10:g.170985301_170985302del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+111_1570+112del MANE Select	ENSP00000326240.4:n.1570+111_1570+112del
ENST00000349841.9:c.1570+111_1570+112del	ENSP00000326240.4:n.1570+111_1570+112del
ENST00000356716.8:c.1570+111_1570+112del	ENSP00000349150.3:n.1570+111_1570+112del
ENST00000544106.5:c.1483+1259_1483+1260del	ENSP00000440637.1:n.1483+1259_1483+1260del
ENST00000602751.5:c.*1178+111_*1178+112del	ENSP00000473654.1:n.*1178+111_*1178+112del
NM_001185118.1:c.1570+111_1570+112del	NP_001172047.1:n.1570+111_1570+112del
NM_001185119.1:c.1483+1259_1483+1260del	NP_001172048.1:n.1483+1259_1483+1260del
NM_018657.4:c.1570+111_1570+112del	NP_061127.1:n.1570+111_1570+112del
NR_033702.1:n.1869+111_1869+112del
NR_033703.1:n.1883+111_1883+112del
XM_005247621.3:c.1486+111_1486+112del	XP_005247678.1:n.1486+111_1486+112del
XM_005247622.3:c.1324+111_1324+112del	XP_005247679.1:n.1324+111_1324+112del
XM_005247624.3:c.1228+111_1228+112del	XP_005247681.1:n.1228+111_1228+112del
XM_011512987.1:c.1570+111_1570+112del	XP_011511289.1:n.1570+111_1570+112del
XM_011512988.1:c.1570+111_1570+112del	XP_011511290.1:n.1570+111_1570+112del
XM_005247621.5:c.1486+111_1486+112del	XP_005247678.1:n.1486+111_1486+112del
XM_005247622.4:c.1324+111_1324+112del	XP_005247679.1:n.1324+111_1324+112del
XM_005247624.4:c.1228+111_1228+112del	XP_005247681.1:n.1228+111_1228+112del
XM_017006864.2:c.1570+111_1570+112del	XP_016862353.1:n.1570+111_1570+112del
XM_017006865.2:c.1144+111_1144+112del	XP_016862354.1:n.1144+111_1144+112del
XM_017006866.2:c.1144+111_1144+112del	XP_016862355.1:n.1144+111_1144+112del
XM_017006867.2:c.751+111_751+112del	XP_016862356.1:n.751+111_751+112del
XM_017006868.2:c.667+111_667+112del	XP_016862357.1:n.667+111_667+112del
XR_002959552.1:n.3402+111_3402+112del
NM_001185118.2:c.1570+111_1570+112del	NP_001172047.1:n.1570+111_1570+112del
NM_018657.5:c.1570+111_1570+112del MANE Select	NP_061127.1:n.1570+111_1570+112del
NR_033702.2:n.1538+111_1538+112del
NR_033703.2:n.1552+111_1552+112del