Canonical Allele Identifier: CA1056197244

Gene: MYNN

Linked Data

• gnomAD v3: 3-169784902-ATCTCT-A
• gnomAD v4: 3-169784902-ATCTCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784904_169784908del , CM000665.2:g.169784904_169784908del	GRCh38
NC_000003.11:g.169502692_169502696del , CM000665.1:g.169502692_169502696del	GRCh37
NC_000003.10:g.170985386_170985390del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+196_1570+200del MANE Select	ENSP00000326240.4:n.1570+196_1570+200del
ENST00000349841.9:c.1570+196_1570+200del	ENSP00000326240.4:n.1570+196_1570+200del
ENST00000356716.8:c.1570+196_1570+200del	ENSP00000349150.3:n.1570+196_1570+200del
ENST00000544106.5:c.1483+1344_1483+1348del	ENSP00000440637.1:n.1483+1344_1483+1348del
ENST00000602751.5:c.*1178+196_*1178+200del	ENSP00000473654.1:n.*1178+196_*1178+200del
NM_001185118.1:c.1570+196_1570+200del	NP_001172047.1:n.1570+196_1570+200del
NM_001185119.1:c.1483+1344_1483+1348del	NP_001172048.1:n.1483+1344_1483+1348del
NM_018657.4:c.1570+196_1570+200del	NP_061127.1:n.1570+196_1570+200del
NR_033702.1:n.1869+196_1869+200del
NR_033703.1:n.1883+196_1883+200del
XM_005247621.3:c.1486+196_1486+200del	XP_005247678.1:n.1486+196_1486+200del
XM_005247622.3:c.1324+196_1324+200del	XP_005247679.1:n.1324+196_1324+200del
XM_005247624.3:c.1228+196_1228+200del	XP_005247681.1:n.1228+196_1228+200del
XM_011512987.1:c.1570+196_1570+200del	XP_011511289.1:n.1570+196_1570+200del
XM_011512988.1:c.1570+196_1570+200del	XP_011511290.1:n.1570+196_1570+200del
XM_005247621.5:c.1486+196_1486+200del	XP_005247678.1:n.1486+196_1486+200del
XM_005247622.4:c.1324+196_1324+200del	XP_005247679.1:n.1324+196_1324+200del
XM_005247624.4:c.1228+196_1228+200del	XP_005247681.1:n.1228+196_1228+200del
XM_017006864.2:c.1570+196_1570+200del	XP_016862353.1:n.1570+196_1570+200del
XM_017006865.2:c.1144+196_1144+200del	XP_016862354.1:n.1144+196_1144+200del
XM_017006866.2:c.1144+196_1144+200del	XP_016862355.1:n.1144+196_1144+200del
XM_017006867.2:c.751+196_751+200del	XP_016862356.1:n.751+196_751+200del
XM_017006868.2:c.667+196_667+200del	XP_016862357.1:n.667+196_667+200del
XR_002959552.1:n.3402+196_3402+200del
NM_001185118.2:c.1570+196_1570+200del	NP_001172047.1:n.1570+196_1570+200del
NM_018657.5:c.1570+196_1570+200del MANE Select	NP_061127.1:n.1570+196_1570+200del
NR_033702.2:n.1538+196_1538+200del
NR_033703.2:n.1552+196_1552+200del