Canonical Allele Identifier: CA436751397

Gene: MYNN

Linked Data

• gnomAD v4: 3-169784701-C-T
• MyVariant Identifiers: chr3:g.169502489C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784701C>T , CM000665.2:g.169784701C>T	GRCh38
NC_000003.11:g.169502489C>T , CM000665.1:g.169502489C>T	GRCh37
NC_000003.10:g.170985183C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1563C>T MANE Select	ENSP00000326240.4:p.Val521=
ENST00000349841.9:c.1563C>T	ENSP00000326240.4:p.Val521=
ENST00000356716.8:c.1563C>T	ENSP00000349150.3:p.Val521=
ENST00000544106.5:c.1483+1141C>T	ENSP00000440637.1:n.1483+1141C>T
ENST00000602751.5:c.*1171C>T	ENSP00000473654.1:n.*1171C>T
NM_001185118.1:c.1563C>T	NP_001172047.1:p.Val521=
NM_001185119.1:c.1483+1141C>T	NP_001172048.1:n.1483+1141C>T
NM_018657.4:c.1563C>T	NP_061127.1:p.Val521=
NR_033702.1:n.1862C>T
NR_033703.1:n.1876C>T
XM_005247621.3:c.1479C>T	XP_005247678.1:p.Val493=
XM_005247622.3:c.1317C>T	XP_005247679.1:p.Val439=
XM_005247624.3:c.1221C>T	XP_005247681.1:p.Val407=
XM_011512987.1:c.1563C>T	XP_011511289.1:p.Val521=
XM_011512988.1:c.1563C>T	XP_011511290.1:p.Val521=
XM_005247621.5:c.1479C>T	XP_005247678.1:p.Val493=
XM_005247622.4:c.1317C>T	XP_005247679.1:p.Val439=
XM_005247624.4:c.1221C>T	XP_005247681.1:p.Val407=
XM_017006864.2:c.1563C>T	XP_016862353.1:p.Val521=
XM_017006865.2:c.1137C>T	XP_016862354.1:p.Val379=
XM_017006866.2:c.1137C>T	XP_016862355.1:p.Val379=
XM_017006867.2:c.744C>T	XP_016862356.1:p.Val248=
XM_017006868.2:c.660C>T	XP_016862357.1:p.Val220=
XR_002959552.1:n.3395C>T
NM_001185118.2:c.1563C>T	NP_001172047.1:p.Val521=
NM_018657.5:c.1563C>T MANE Select	NP_061127.1:p.Val521=
NR_033702.2:n.1531C>T
NR_033703.2:n.1545C>T