Canonical Allele Identifier: CA355067268

Gene: MYNN

Linked Data

• MyVariant Identifiers: chr3:g.169502493T>A (hg19) ; chr3:g.169784705T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784705T>A , CM000665.2:g.169784705T>A	GRCh38
NC_000003.11:g.169502493T>A , CM000665.1:g.169502493T>A	GRCh37
NC_000003.10:g.170985187T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1567T>A MANE Select	ENSP00000326240.4:p.Ser523Thr
ENST00000349841.9:c.1567T>A	ENSP00000326240.4:p.Ser523Thr
ENST00000356716.8:c.1567T>A	ENSP00000349150.3:p.Ser523Thr
ENST00000544106.5:c.1483+1145T>A	ENSP00000440637.1:n.1483+1145T>A
ENST00000602751.5:c.*1175T>A	ENSP00000473654.1:n.*1175T>A
NM_001185118.1:c.1567T>A	NP_001172047.1:p.Ser523Thr
NM_001185119.1:c.1483+1145T>A	NP_001172048.1:n.1483+1145T>A
NM_018657.4:c.1567T>A	NP_061127.1:p.Ser523Thr
NR_033702.1:n.1866T>A
NR_033703.1:n.1880T>A
XM_005247621.3:c.1483T>A	XP_005247678.1:p.Ser495Thr
XM_005247622.3:c.1321T>A	XP_005247679.1:p.Ser441Thr
XM_005247624.3:c.1225T>A	XP_005247681.1:p.Ser409Thr
XM_011512987.1:c.1567T>A	XP_011511289.1:p.Ser523Thr
XM_011512988.1:c.1567T>A	XP_011511290.1:p.Ser523Thr
XM_005247621.5:c.1483T>A	XP_005247678.1:p.Ser495Thr
XM_005247622.4:c.1321T>A	XP_005247679.1:p.Ser441Thr
XM_005247624.4:c.1225T>A	XP_005247681.1:p.Ser409Thr
XM_017006864.2:c.1567T>A	XP_016862353.1:p.Ser523Thr
XM_017006865.2:c.1141T>A	XP_016862354.1:p.Ser381Thr
XM_017006866.2:c.1141T>A	XP_016862355.1:p.Ser381Thr
XM_017006867.2:c.748T>A	XP_016862356.1:p.Ser250Thr
XM_017006868.2:c.664T>A	XP_016862357.1:p.Ser222Thr
XR_002959552.1:n.3399T>A
NM_001185118.2:c.1567T>A	NP_001172047.1:p.Ser523Thr
NM_018657.5:c.1567T>A MANE Select	NP_061127.1:p.Ser523Thr
NR_033702.2:n.1535T>A
NR_033703.2:n.1549T>A