Canonical Allele Identifier: CA2668475185

Gene: MYNN

Linked Data

• gnomAD v4: 3-169784806-CAGTTTAAATTAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784808_169784819del , CM000665.2:g.169784808_169784819del	GRCh38
NC_000003.11:g.169502596_169502607del , CM000665.1:g.169502596_169502607del	GRCh37
NC_000003.10:g.170985290_170985301del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+100_1570+111del MANE Select	ENSP00000326240.4:n.1570+100_1570+111del
ENST00000349841.9:c.1570+100_1570+111del	ENSP00000326240.4:n.1570+100_1570+111del
ENST00000356716.8:c.1570+100_1570+111del	ENSP00000349150.3:n.1570+100_1570+111del
ENST00000544106.5:c.1483+1248_1483+1259del	ENSP00000440637.1:n.1483+1248_1483+1259del
ENST00000602751.5:c.*1178+100_*1178+111del	ENSP00000473654.1:n.*1178+100_*1178+111del
NM_001185118.1:c.1570+100_1570+111del	NP_001172047.1:n.1570+100_1570+111del
NM_001185119.1:c.1483+1248_1483+1259del	NP_001172048.1:n.1483+1248_1483+1259del
NM_018657.4:c.1570+100_1570+111del	NP_061127.1:n.1570+100_1570+111del
NR_033702.1:n.1869+100_1869+111del
NR_033703.1:n.1883+100_1883+111del
XM_005247621.3:c.1486+100_1486+111del	XP_005247678.1:n.1486+100_1486+111del
XM_005247622.3:c.1324+100_1324+111del	XP_005247679.1:n.1324+100_1324+111del
XM_005247624.3:c.1228+100_1228+111del	XP_005247681.1:n.1228+100_1228+111del
XM_011512987.1:c.1570+100_1570+111del	XP_011511289.1:n.1570+100_1570+111del
XM_011512988.1:c.1570+100_1570+111del	XP_011511290.1:n.1570+100_1570+111del
XM_005247621.5:c.1486+100_1486+111del	XP_005247678.1:n.1486+100_1486+111del
XM_005247622.4:c.1324+100_1324+111del	XP_005247679.1:n.1324+100_1324+111del
XM_005247624.4:c.1228+100_1228+111del	XP_005247681.1:n.1228+100_1228+111del
XM_017006864.2:c.1570+100_1570+111del	XP_016862353.1:n.1570+100_1570+111del
XM_017006865.2:c.1144+100_1144+111del	XP_016862354.1:n.1144+100_1144+111del
XM_017006866.2:c.1144+100_1144+111del	XP_016862355.1:n.1144+100_1144+111del
XM_017006867.2:c.751+100_751+111del	XP_016862356.1:n.751+100_751+111del
XM_017006868.2:c.667+100_667+111del	XP_016862357.1:n.667+100_667+111del
XR_002959552.1:n.3402+100_3402+111del
NM_001185118.2:c.1570+100_1570+111del	NP_001172047.1:n.1570+100_1570+111del
NM_018657.5:c.1570+100_1570+111del MANE Select	NP_061127.1:n.1570+100_1570+111del
NR_033702.2:n.1538+100_1538+111del
NR_033703.2:n.1552+100_1552+111del