Canonical Allele Identifier: CA1419592911

Gene: MYNN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169779738T= , CM000665.2:g.169779738T=	GRCh38
NC_000003.11:g.169497526T= , CM000665.1:g.169497526T=	GRCh37
NC_000003.10:g.170980220T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1060+177T= MANE Select	ENSP00000326240.4:n.1060+177T=
ENST00000349841.9:c.1060+177T=	ENSP00000326240.4:n.1060+177T=
ENST00000356716.8:c.1060+177T=	ENSP00000349150.3:n.1060+177T=
ENST00000544106.5:c.1060+177T=	ENSP00000440637.1:n.1060+177T=
ENST00000602391.1:c.273+177T=
ENST00000602751.5:c.*668+177T=	ENSP00000473654.1:n.*668+177T=
NM_001185118.1:c.1060+177T=	NP_001172047.1:n.1060+177T=
NM_001185119.1:c.1060+177T=	NP_001172048.1:n.1060+177T=
NM_018657.4:c.1060+177T=	NP_061127.1:n.1060+177T=
NR_033702.1:n.1359+177T=
NR_033703.1:n.1373+177T=
XM_005247621.3:c.1060+177T=	XP_005247678.1:n.1060+177T=
XM_005247622.3:c.814+177T=	XP_005247679.1:n.814+177T=
XM_005247624.3:c.718+177T=	XP_005247681.1:n.718+177T=
XM_011512987.1:c.1060+177T=	XP_011511289.1:n.1060+177T=
XM_011512988.1:c.1060+177T=	XP_011511290.1:n.1060+177T=
XM_005247621.5:c.1060+177T=	XP_005247678.1:n.1060+177T=
XM_005247622.4:c.814+177T=	XP_005247679.1:n.814+177T=
XM_005247624.4:c.718+177T=	XP_005247681.1:n.718+177T=
XM_017006864.2:c.1060+177T=	XP_016862353.1:n.1060+177T=
XM_017006865.2:c.718+177T=	XP_016862354.1:n.718+177T=
XM_017006866.2:c.718+177T=	XP_016862355.1:n.718+177T=
XM_017006867.2:c.241+177T=	XP_016862356.1:n.241+177T=
XM_017006868.2:c.241+177T=	XP_016862357.1:n.241+177T=
XR_002959552.1:n.1761+177T=
NM_001185118.2:c.1060+177T=	NP_001172047.1:n.1060+177T=
NM_018657.5:c.1060+177T= MANE Select	NP_061127.1:n.1060+177T=
NR_033702.2:n.1028+177T=
NR_033703.2:n.1042+177T=