Canonical Allele Identifier: CA2668475205

Gene: MYNN

Linked Data

• gnomAD v4: 3-169784815-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784815_169784816insG , CM000665.2:g.169784815_169784816insG	GRCh38
NC_000003.11:g.169502603_169502604insG , CM000665.1:g.169502603_169502604insG	GRCh37
NC_000003.10:g.170985297_170985298insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+107_1570+108insG MANE Select	ENSP00000326240.4:n.1570+107_1570+108insG
ENST00000349841.9:c.1570+107_1570+108insG	ENSP00000326240.4:n.1570+107_1570+108insG
ENST00000356716.8:c.1570+107_1570+108insG	ENSP00000349150.3:n.1570+107_1570+108insG
ENST00000544106.5:c.1483+1255_1483+1256insG	ENSP00000440637.1:n.1483+1255_1483+1256insG
ENST00000602751.5:c.*1178+107_*1178+108insG	ENSP00000473654.1:n.*1178+107_*1178+108insG
NM_001185118.1:c.1570+107_1570+108insG	NP_001172047.1:n.1570+107_1570+108insG
NM_001185119.1:c.1483+1255_1483+1256insG	NP_001172048.1:n.1483+1255_1483+1256insG
NM_018657.4:c.1570+107_1570+108insG	NP_061127.1:n.1570+107_1570+108insG
NR_033702.1:n.1869+107_1869+108insG
NR_033703.1:n.1883+107_1883+108insG
XM_005247621.3:c.1486+107_1486+108insG	XP_005247678.1:n.1486+107_1486+108insG
XM_005247622.3:c.1324+107_1324+108insG	XP_005247679.1:n.1324+107_1324+108insG
XM_005247624.3:c.1228+107_1228+108insG	XP_005247681.1:n.1228+107_1228+108insG
XM_011512987.1:c.1570+107_1570+108insG	XP_011511289.1:n.1570+107_1570+108insG
XM_011512988.1:c.1570+107_1570+108insG	XP_011511290.1:n.1570+107_1570+108insG
XM_005247621.5:c.1486+107_1486+108insG	XP_005247678.1:n.1486+107_1486+108insG
XM_005247622.4:c.1324+107_1324+108insG	XP_005247679.1:n.1324+107_1324+108insG
XM_005247624.4:c.1228+107_1228+108insG	XP_005247681.1:n.1228+107_1228+108insG
XM_017006864.2:c.1570+107_1570+108insG	XP_016862353.1:n.1570+107_1570+108insG
XM_017006865.2:c.1144+107_1144+108insG	XP_016862354.1:n.1144+107_1144+108insG
XM_017006866.2:c.1144+107_1144+108insG	XP_016862355.1:n.1144+107_1144+108insG
XM_017006867.2:c.751+107_751+108insG	XP_016862356.1:n.751+107_751+108insG
XM_017006868.2:c.667+107_667+108insG	XP_016862357.1:n.667+107_667+108insG
XR_002959552.1:n.3402+107_3402+108insG
NM_001185118.2:c.1570+107_1570+108insG	NP_001172047.1:n.1570+107_1570+108insG
NM_018657.5:c.1570+107_1570+108insG MANE Select	NP_061127.1:n.1570+107_1570+108insG
NR_033702.2:n.1538+107_1538+108insG
NR_033703.2:n.1552+107_1552+108insG