Canonical Allele Identifier: CA355067234

Gene: MYNN

Linked Data

• gnomAD v3: 3-169784700-T-C
• gnomAD v4: 3-169784700-T-C
• MyVariant Identifiers: chr3:g.169502488T>C (hg19) ; chr3:g.169784700T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784700T>C , CM000665.2:g.169784700T>C	GRCh38
NC_000003.11:g.169502488T>C , CM000665.1:g.169502488T>C	GRCh37
NC_000003.10:g.170985182T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1562T>C MANE Select	ENSP00000326240.4:p.Val521Ala
ENST00000349841.9:c.1562T>C	ENSP00000326240.4:p.Val521Ala
ENST00000356716.8:c.1562T>C	ENSP00000349150.3:p.Val521Ala
ENST00000544106.5:c.1483+1140T>C	ENSP00000440637.1:n.1483+1140T>C
ENST00000602751.5:c.*1170T>C	ENSP00000473654.1:n.*1170T>C
NM_001185118.1:c.1562T>C	NP_001172047.1:p.Val521Ala
NM_001185119.1:c.1483+1140T>C	NP_001172048.1:n.1483+1140T>C
NM_018657.4:c.1562T>C	NP_061127.1:p.Val521Ala
NR_033702.1:n.1861T>C
NR_033703.1:n.1875T>C
XM_005247621.3:c.1478T>C	XP_005247678.1:p.Val493Ala
XM_005247622.3:c.1316T>C	XP_005247679.1:p.Val439Ala
XM_005247624.3:c.1220T>C	XP_005247681.1:p.Val407Ala
XM_011512987.1:c.1562T>C	XP_011511289.1:p.Val521Ala
XM_011512988.1:c.1562T>C	XP_011511290.1:p.Val521Ala
XM_005247621.5:c.1478T>C	XP_005247678.1:p.Val493Ala
XM_005247622.4:c.1316T>C	XP_005247679.1:p.Val439Ala
XM_005247624.4:c.1220T>C	XP_005247681.1:p.Val407Ala
XM_017006864.2:c.1562T>C	XP_016862353.1:p.Val521Ala
XM_017006865.2:c.1136T>C	XP_016862354.1:p.Val379Ala
XM_017006866.2:c.1136T>C	XP_016862355.1:p.Val379Ala
XM_017006867.2:c.743T>C	XP_016862356.1:p.Val248Ala
XM_017006868.2:c.659T>C	XP_016862357.1:p.Val220Ala
XR_002959552.1:n.3394T>C
NM_001185118.2:c.1562T>C	NP_001172047.1:p.Val521Ala
NM_018657.5:c.1562T>C MANE Select	NP_061127.1:p.Val521Ala
NR_033702.2:n.1530T>C
NR_033703.2:n.1544T>C