Canonical Allele Identifier: CA2563671358

Gene: MYNN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784875_169784876insTAGA , CM000665.2:g.169784875_169784876insTAGA	GRCh38
NC_000003.11:g.169502663_169502664insTAGA , CM000665.1:g.169502663_169502664insTAGA	GRCh37
NC_000003.10:g.170985357_170985358insTAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+167_1570+168insTAGA MANE Select	ENSP00000326240.4:n.1570+167_1570+168insTAGA
ENST00000349841.9:c.1570+167_1570+168insTAGA	ENSP00000326240.4:n.1570+167_1570+168insTAGA
ENST00000356716.8:c.1570+167_1570+168insTAGA	ENSP00000349150.3:n.1570+167_1570+168insTAGA
ENST00000544106.5:c.1483+1315_1483+1316insTAGA	ENSP00000440637.1:n.1483+1315_1483+1316insTAGA
ENST00000602751.5:c.*1178+167_*1178+168insTAGA	ENSP00000473654.1:n.*1178+167_*1178+168insTAGA
NM_001185118.1:c.1570+167_1570+168insTAGA	NP_001172047.1:n.1570+167_1570+168insTAGA
NM_001185119.1:c.1483+1315_1483+1316insTAGA	NP_001172048.1:n.1483+1315_1483+1316insTAGA
NM_018657.4:c.1570+167_1570+168insTAGA	NP_061127.1:n.1570+167_1570+168insTAGA
NR_033702.1:n.1869+167_1869+168insTAGA
NR_033703.1:n.1883+167_1883+168insTAGA
XM_005247621.3:c.1486+167_1486+168insTAGA	XP_005247678.1:n.1486+167_1486+168insTAGA
XM_005247622.3:c.1324+167_1324+168insTAGA	XP_005247679.1:n.1324+167_1324+168insTAGA
XM_005247624.3:c.1228+167_1228+168insTAGA	XP_005247681.1:n.1228+167_1228+168insTAGA
XM_011512987.1:c.1570+167_1570+168insTAGA	XP_011511289.1:n.1570+167_1570+168insTAGA
XM_011512988.1:c.1570+167_1570+168insTAGA	XP_011511290.1:n.1570+167_1570+168insTAGA
XM_005247621.5:c.1486+167_1486+168insTAGA	XP_005247678.1:n.1486+167_1486+168insTAGA
XM_005247622.4:c.1324+167_1324+168insTAGA	XP_005247679.1:n.1324+167_1324+168insTAGA
XM_005247624.4:c.1228+167_1228+168insTAGA	XP_005247681.1:n.1228+167_1228+168insTAGA
XM_017006864.2:c.1570+167_1570+168insTAGA	XP_016862353.1:n.1570+167_1570+168insTAGA
XM_017006865.2:c.1144+167_1144+168insTAGA	XP_016862354.1:n.1144+167_1144+168insTAGA
XM_017006866.2:c.1144+167_1144+168insTAGA	XP_016862355.1:n.1144+167_1144+168insTAGA
XM_017006867.2:c.751+167_751+168insTAGA	XP_016862356.1:n.751+167_751+168insTAGA
XM_017006868.2:c.667+167_667+168insTAGA	XP_016862357.1:n.667+167_667+168insTAGA
XR_002959552.1:n.3402+167_3402+168insTAGA
NM_001185118.2:c.1570+167_1570+168insTAGA	NP_001172047.1:n.1570+167_1570+168insTAGA
NM_018657.5:c.1570+167_1570+168insTAGA MANE Select	NP_061127.1:n.1570+167_1570+168insTAGA
NR_033702.2:n.1538+167_1538+168insTAGA
NR_033703.2:n.1552+167_1552+168insTAGA