Canonical Allele Identifier: CA2697410

Gene: MYNN

Linked Data

• dbSNP Id: rs371285454
• ExAC: 3:169502519 CTTGT / C
• gnomAD v2: 3-169502519-CTTGT-C
• gnomAD v3: 3-169784731-CTTGT-C
• gnomAD v4: 3-169784731-CTTGT-C
• MyVariant Identifiers: chr3:g.169502520_169502523del (hg19) ; chr3:g.169784732_169784735del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784742_169784745del , CM000665.2:g.169784742_169784745del	GRCh38
NC_000003.11:g.169502530_169502533del , CM000665.1:g.169502530_169502533del	GRCh37
NC_000003.10:g.170985224_170985227del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+34_1570+37del MANE Select	ENSP00000326240.4:n.1570+34_1570+37del
ENST00000349841.9:c.1570+34_1570+37del	ENSP00000326240.4:n.1570+34_1570+37del
ENST00000356716.8:c.1570+34_1570+37del	ENSP00000349150.3:n.1570+34_1570+37del
ENST00000544106.5:c.1483+1182_1483+1185del	ENSP00000440637.1:n.1483+1182_1483+1185del
ENST00000602751.5:c.*1178+34_*1178+37del	ENSP00000473654.1:n.*1178+34_*1178+37del
NM_001185118.1:c.1570+34_1570+37del	NP_001172047.1:n.1570+34_1570+37del
NM_001185119.1:c.1483+1182_1483+1185del	NP_001172048.1:n.1483+1182_1483+1185del
NM_018657.4:c.1570+34_1570+37del	NP_061127.1:n.1570+34_1570+37del
NR_033702.1:n.1869+34_1869+37del
NR_033703.1:n.1883+34_1883+37del
XM_005247621.3:c.1486+34_1486+37del	XP_005247678.1:n.1486+34_1486+37del
XM_005247622.3:c.1324+34_1324+37del	XP_005247679.1:n.1324+34_1324+37del
XM_005247624.3:c.1228+34_1228+37del	XP_005247681.1:n.1228+34_1228+37del
XM_011512987.1:c.1570+34_1570+37del	XP_011511289.1:n.1570+34_1570+37del
XM_011512988.1:c.1570+34_1570+37del	XP_011511290.1:n.1570+34_1570+37del
XM_005247621.5:c.1486+34_1486+37del	XP_005247678.1:n.1486+34_1486+37del
XM_005247622.4:c.1324+34_1324+37del	XP_005247679.1:n.1324+34_1324+37del
XM_005247624.4:c.1228+34_1228+37del	XP_005247681.1:n.1228+34_1228+37del
XM_017006864.2:c.1570+34_1570+37del	XP_016862353.1:n.1570+34_1570+37del
XM_017006865.2:c.1144+34_1144+37del	XP_016862354.1:n.1144+34_1144+37del
XM_017006866.2:c.1144+34_1144+37del	XP_016862355.1:n.1144+34_1144+37del
XM_017006867.2:c.751+34_751+37del	XP_016862356.1:n.751+34_751+37del
XM_017006868.2:c.667+34_667+37del	XP_016862357.1:n.667+34_667+37del
XR_002959552.1:n.3402+34_3402+37del
NM_001185118.2:c.1570+34_1570+37del	NP_001172047.1:n.1570+34_1570+37del
NM_018657.5:c.1570+34_1570+37del MANE Select	NP_061127.1:n.1570+34_1570+37del
NR_033702.2:n.1538+34_1538+37del
NR_033703.2:n.1552+34_1552+37del