Canonical Allele Identifier: CA355067228

Gene: MYNN

Linked Data

• gnomAD v4: 3-169784699-G-A
• MyVariant Identifiers: chr3:g.169502487G>A (hg19) ; chr3:g.169784699G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784699G>A , CM000665.2:g.169784699G>A	GRCh38
NC_000003.11:g.169502487G>A , CM000665.1:g.169502487G>A	GRCh37
NC_000003.10:g.170985181G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1561G>A MANE Select	ENSP00000326240.4:p.Val521Ile
ENST00000349841.9:c.1561G>A	ENSP00000326240.4:p.Val521Ile
ENST00000356716.8:c.1561G>A	ENSP00000349150.3:p.Val521Ile
ENST00000544106.5:c.1483+1139G>A	ENSP00000440637.1:n.1483+1139G>A
ENST00000602751.5:c.*1169G>A	ENSP00000473654.1:n.*1169G>A
NM_001185118.1:c.1561G>A	NP_001172047.1:p.Val521Ile
NM_001185119.1:c.1483+1139G>A	NP_001172048.1:n.1483+1139G>A
NM_018657.4:c.1561G>A	NP_061127.1:p.Val521Ile
NR_033702.1:n.1860G>A
NR_033703.1:n.1874G>A
XM_005247621.3:c.1477G>A	XP_005247678.1:p.Val493Ile
XM_005247622.3:c.1315G>A	XP_005247679.1:p.Val439Ile
XM_005247624.3:c.1219G>A	XP_005247681.1:p.Val407Ile
XM_011512987.1:c.1561G>A	XP_011511289.1:p.Val521Ile
XM_011512988.1:c.1561G>A	XP_011511290.1:p.Val521Ile
XM_005247621.5:c.1477G>A	XP_005247678.1:p.Val493Ile
XM_005247622.4:c.1315G>A	XP_005247679.1:p.Val439Ile
XM_005247624.4:c.1219G>A	XP_005247681.1:p.Val407Ile
XM_017006864.2:c.1561G>A	XP_016862353.1:p.Val521Ile
XM_017006865.2:c.1135G>A	XP_016862354.1:p.Val379Ile
XM_017006866.2:c.1135G>A	XP_016862355.1:p.Val379Ile
XM_017006867.2:c.742G>A	XP_016862356.1:p.Val248Ile
XM_017006868.2:c.658G>A	XP_016862357.1:p.Val220Ile
XR_002959552.1:n.3393G>A
NM_001185118.2:c.1561G>A	NP_001172047.1:p.Val521Ile
NM_018657.5:c.1561G>A MANE Select	NP_061127.1:p.Val521Ile
NR_033702.2:n.1529G>A
NR_033703.2:n.1543G>A