Canonical Allele Identifier: CA902413133

Gene: MYNN

Linked Data

• dbSNP Id: rs1202270066
• MyVariant Identifiers: chr3:g.169502634_169502635insAT (hg19) ; chr3:g.169784846_169784847insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784847_169784848dup , CM000665.2:g.169784847_169784848dup	GRCh38
NC_000003.11:g.169502635_169502636dup , CM000665.1:g.169502635_169502636dup	GRCh37
NC_000003.10:g.170985329_170985330dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+139_1570+140dup MANE Select	ENSP00000326240.4:n.1570+139_1570+140dup
ENST00000349841.9:c.1570+139_1570+140dup	ENSP00000326240.4:n.1570+139_1570+140dup
ENST00000356716.8:c.1570+139_1570+140dup	ENSP00000349150.3:n.1570+139_1570+140dup
ENST00000544106.5:c.1483+1287_1483+1288dup	ENSP00000440637.1:n.1483+1287_1483+1288dup
ENST00000602751.5:c.*1178+139_*1178+140dup	ENSP00000473654.1:n.*1178+139_*1178+140dup
NM_001185118.1:c.1570+139_1570+140dup	NP_001172047.1:n.1570+139_1570+140dup
NM_001185119.1:c.1483+1287_1483+1288dup	NP_001172048.1:n.1483+1287_1483+1288dup
NM_018657.4:c.1570+139_1570+140dup	NP_061127.1:n.1570+139_1570+140dup
NR_033702.1:n.1869+139_1869+140dup
NR_033703.1:n.1883+139_1883+140dup
XM_005247621.3:c.1486+139_1486+140dup	XP_005247678.1:n.1486+139_1486+140dup
XM_005247622.3:c.1324+139_1324+140dup	XP_005247679.1:n.1324+139_1324+140dup
XM_005247624.3:c.1228+139_1228+140dup	XP_005247681.1:n.1228+139_1228+140dup
XM_011512987.1:c.1570+139_1570+140dup	XP_011511289.1:n.1570+139_1570+140dup
XM_011512988.1:c.1570+139_1570+140dup	XP_011511290.1:n.1570+139_1570+140dup
XM_005247621.5:c.1486+139_1486+140dup	XP_005247678.1:n.1486+139_1486+140dup
XM_005247622.4:c.1324+139_1324+140dup	XP_005247679.1:n.1324+139_1324+140dup
XM_005247624.4:c.1228+139_1228+140dup	XP_005247681.1:n.1228+139_1228+140dup
XM_017006864.2:c.1570+139_1570+140dup	XP_016862353.1:n.1570+139_1570+140dup
XM_017006865.2:c.1144+139_1144+140dup	XP_016862354.1:n.1144+139_1144+140dup
XM_017006866.2:c.1144+139_1144+140dup	XP_016862355.1:n.1144+139_1144+140dup
XM_017006867.2:c.751+139_751+140dup	XP_016862356.1:n.751+139_751+140dup
XM_017006868.2:c.667+139_667+140dup	XP_016862357.1:n.667+139_667+140dup
XR_002959552.1:n.3402+139_3402+140dup
NM_001185118.2:c.1570+139_1570+140dup	NP_001172047.1:n.1570+139_1570+140dup
NM_018657.5:c.1570+139_1570+140dup MANE Select	NP_061127.1:n.1570+139_1570+140dup
NR_033702.2:n.1538+139_1538+140dup
NR_033703.2:n.1552+139_1552+140dup