Canonical Allele Identifier: CA2830535911

Gene: MYNN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784797del , CM000665.2:g.169784797del	GRCh38
NC_000003.11:g.169502585del , CM000665.1:g.169502585del	GRCh37
NC_000003.10:g.170985279del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+89del MANE Select	ENSP00000326240.4:n.1570+89del
ENST00000349841.9:c.1570+89del	ENSP00000326240.4:n.1570+89del
ENST00000356716.8:c.1570+89del	ENSP00000349150.3:n.1570+89del
ENST00000544106.5:c.1483+1237del	ENSP00000440637.1:n.1483+1237del
ENST00000602751.5:c.*1178+89del	ENSP00000473654.1:n.*1178+89del
NM_001185118.1:c.1570+89del	NP_001172047.1:n.1570+89del
NM_001185119.1:c.1483+1237del	NP_001172048.1:n.1483+1237del
NM_018657.4:c.1570+89del	NP_061127.1:n.1570+89del
NR_033702.1:n.1869+89del
NR_033703.1:n.1883+89del
XM_005247621.3:c.1486+89del	XP_005247678.1:n.1486+89del
XM_005247622.3:c.1324+89del	XP_005247679.1:n.1324+89del
XM_005247624.3:c.1228+89del	XP_005247681.1:n.1228+89del
XM_011512987.1:c.1570+89del	XP_011511289.1:n.1570+89del
XM_011512988.1:c.1570+89del	XP_011511290.1:n.1570+89del
XM_005247621.5:c.1486+89del	XP_005247678.1:n.1486+89del
XM_005247622.4:c.1324+89del	XP_005247679.1:n.1324+89del
XM_005247624.4:c.1228+89del	XP_005247681.1:n.1228+89del
XM_017006864.2:c.1570+89del	XP_016862353.1:n.1570+89del
XM_017006865.2:c.1144+89del	XP_016862354.1:n.1144+89del
XM_017006866.2:c.1144+89del	XP_016862355.1:n.1144+89del
XM_017006867.2:c.751+89del	XP_016862356.1:n.751+89del
XM_017006868.2:c.667+89del	XP_016862357.1:n.667+89del
XR_002959552.1:n.3402+89del
NM_001185118.2:c.1570+89del	NP_001172047.1:n.1570+89del
NM_018657.5:c.1570+89del MANE Select	NP_061127.1:n.1570+89del
NR_033702.2:n.1538+89del
NR_033703.2:n.1552+89del