Canonical Allele Identifier: CA902409081

Gene: MYNN

Linked Data

• dbSNP Id: rs1314929417
• gnomAD v4: 3-169779764-C-CATTAGGGT
• MyVariant Identifiers: chr3:g.169497552_169497553insATTAGGGT (hg19) ; chr3:g.169779764_169779765insATTAGGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169779765_169779766insTTAGGGTA , CM000665.2:g.169779765_169779766insTTAGGGTA	GRCh38
NC_000003.11:g.169497553_169497554insTTAGGGTA , CM000665.1:g.169497553_169497554insTTAGGGTA	GRCh37
NC_000003.10:g.170980247_170980248insTTAGGGTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1060+204_1060+205insTTAGGGTA MANE Select	ENSP00000326240.4:n.1060+204_1060+205insTTAGGGTA
ENST00000349841.9:c.1060+204_1060+205insTTAGGGTA	ENSP00000326240.4:n.1060+204_1060+205insTTAGGGTA
ENST00000356716.8:c.1060+204_1060+205insTTAGGGTA	ENSP00000349150.3:n.1060+204_1060+205insTTAGGGTA
ENST00000544106.5:c.1060+204_1060+205insTTAGGGTA	ENSP00000440637.1:n.1060+204_1060+205insTTAGGGTA
ENST00000602391.1:c.273+204_273+205insTTAGGGTA
ENST00000602751.5:c.*668+204_*668+205insTTAGGGTA	ENSP00000473654.1:n.*668+204_*668+205insTTAGGGTA
NM_001185118.1:c.1060+204_1060+205insTTAGGGTA	NP_001172047.1:n.1060+204_1060+205insTTAGGGTA
NM_001185119.1:c.1060+204_1060+205insTTAGGGTA	NP_001172048.1:n.1060+204_1060+205insTTAGGGTA
NM_018657.4:c.1060+204_1060+205insTTAGGGTA	NP_061127.1:n.1060+204_1060+205insTTAGGGTA
NR_033702.1:n.1359+204_1359+205insTTAGGGTA
NR_033703.1:n.1373+204_1373+205insTTAGGGTA
XM_005247621.3:c.1060+204_1060+205insTTAGGGTA	XP_005247678.1:n.1060+204_1060+205insTTAGGGTA
XM_005247622.3:c.814+204_814+205insTTAGGGTA	XP_005247679.1:n.814+204_814+205insTTAGGGTA
XM_005247624.3:c.718+204_718+205insTTAGGGTA	XP_005247681.1:n.718+204_718+205insTTAGGGTA
XM_011512987.1:c.1060+204_1060+205insTTAGGGTA	XP_011511289.1:n.1060+204_1060+205insTTAGGGTA
XM_011512988.1:c.1060+204_1060+205insTTAGGGTA	XP_011511290.1:n.1060+204_1060+205insTTAGGGTA
XM_005247621.5:c.1060+204_1060+205insTTAGGGTA	XP_005247678.1:n.1060+204_1060+205insTTAGGGTA
XM_005247622.4:c.814+204_814+205insTTAGGGTA	XP_005247679.1:n.814+204_814+205insTTAGGGTA
XM_005247624.4:c.718+204_718+205insTTAGGGTA	XP_005247681.1:n.718+204_718+205insTTAGGGTA
XM_017006864.2:c.1060+204_1060+205insTTAGGGTA	XP_016862353.1:n.1060+204_1060+205insTTAGGGTA
XM_017006865.2:c.718+204_718+205insTTAGGGTA	XP_016862354.1:n.718+204_718+205insTTAGGGTA
XM_017006866.2:c.718+204_718+205insTTAGGGTA	XP_016862355.1:n.718+204_718+205insTTAGGGTA
XM_017006867.2:c.241+204_241+205insTTAGGGTA	XP_016862356.1:n.241+204_241+205insTTAGGGTA
XM_017006868.2:c.241+204_241+205insTTAGGGTA	XP_016862357.1:n.241+204_241+205insTTAGGGTA
XR_002959552.1:n.1761+204_1761+205insTTAGGGTA
NM_001185118.2:c.1060+204_1060+205insTTAGGGTA	NP_001172047.1:n.1060+204_1060+205insTTAGGGTA
NM_018657.5:c.1060+204_1060+205insTTAGGGTA MANE Select	NP_061127.1:n.1060+204_1060+205insTTAGGGTA
NR_033702.2:n.1028+204_1028+205insTTAGGGTA
NR_033703.2:n.1042+204_1042+205insTTAGGGTA