Canonical Allele Identifier: CA87595644

Gene: MYNN

Linked Data

• dbSNP Id: rs35197165
• gnomAD v2: 3-169497554-A-ACT
• gnomAD v3: 3-169779766-A-ACT
• gnomAD v4: 3-169779766-A-ACT
• MyVariant Identifiers: chr3:g.169497557_169497558insTC (hg19) ; chr3:g.169497554_169497555insCT (hg19) ; chr3:g.169779769_169779770insTC (hg38) ; chr3:g.169779766_169779767insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169779768_169779769dup , CM000665.2:g.169779768_169779769dup	GRCh38
NC_000003.11:g.169497556_169497557dup , CM000665.1:g.169497556_169497557dup	GRCh37
NC_000003.10:g.170980250_170980251dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1060+207_1060+208dup MANE Select	ENSP00000326240.4:n.1060+207_1060+208dup
ENST00000349841.9:c.1060+207_1060+208dup	ENSP00000326240.4:n.1060+207_1060+208dup
ENST00000356716.8:c.1060+207_1060+208dup	ENSP00000349150.3:n.1060+207_1060+208dup
ENST00000544106.5:c.1060+207_1060+208dup	ENSP00000440637.1:n.1060+207_1060+208dup
ENST00000602391.1:c.273+207_273+208dup
ENST00000602751.5:c.*668+207_*668+208dup	ENSP00000473654.1:n.*668+207_*668+208dup
NM_001185118.1:c.1060+207_1060+208dup	NP_001172047.1:n.1060+207_1060+208dup
NM_001185119.1:c.1060+207_1060+208dup	NP_001172048.1:n.1060+207_1060+208dup
NM_018657.4:c.1060+207_1060+208dup	NP_061127.1:n.1060+207_1060+208dup
NR_033702.1:n.1359+207_1359+208dup
NR_033703.1:n.1373+207_1373+208dup
XM_005247621.3:c.1060+207_1060+208dup	XP_005247678.1:n.1060+207_1060+208dup
XM_005247622.3:c.814+207_814+208dup	XP_005247679.1:n.814+207_814+208dup
XM_005247624.3:c.718+207_718+208dup	XP_005247681.1:n.718+207_718+208dup
XM_011512987.1:c.1060+207_1060+208dup	XP_011511289.1:n.1060+207_1060+208dup
XM_011512988.1:c.1060+207_1060+208dup	XP_011511290.1:n.1060+207_1060+208dup
XM_005247621.5:c.1060+207_1060+208dup	XP_005247678.1:n.1060+207_1060+208dup
XM_005247622.4:c.814+207_814+208dup	XP_005247679.1:n.814+207_814+208dup
XM_005247624.4:c.718+207_718+208dup	XP_005247681.1:n.718+207_718+208dup
XM_017006864.2:c.1060+207_1060+208dup	XP_016862353.1:n.1060+207_1060+208dup
XM_017006865.2:c.718+207_718+208dup	XP_016862354.1:n.718+207_718+208dup
XM_017006866.2:c.718+207_718+208dup	XP_016862355.1:n.718+207_718+208dup
XM_017006867.2:c.241+207_241+208dup	XP_016862356.1:n.241+207_241+208dup
XM_017006868.2:c.241+207_241+208dup	XP_016862357.1:n.241+207_241+208dup
XR_002959552.1:n.1761+207_1761+208dup
NM_001185118.2:c.1060+207_1060+208dup	NP_001172047.1:n.1060+207_1060+208dup
NM_018657.5:c.1060+207_1060+208dup MANE Select	NP_061127.1:n.1060+207_1060+208dup
NR_033702.2:n.1028+207_1028+208dup
NR_033703.2:n.1042+207_1042+208dup