Canonical Allele Identifier: CA2830535913

Gene: MYNN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784803A>C , CM000665.2:g.169784803A>C	GRCh38
NC_000003.11:g.169502591A>C , CM000665.1:g.169502591A>C	GRCh37
NC_000003.10:g.170985285A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570+95A>C MANE Select	ENSP00000326240.4:n.1570+95A>C
ENST00000349841.9:c.1570+95A>C	ENSP00000326240.4:n.1570+95A>C
ENST00000356716.8:c.1570+95A>C	ENSP00000349150.3:n.1570+95A>C
ENST00000544106.5:c.1483+1243A>C	ENSP00000440637.1:n.1483+1243A>C
ENST00000602751.5:c.*1178+95A>C	ENSP00000473654.1:n.*1178+95A>C
NM_001185118.1:c.1570+95A>C	NP_001172047.1:n.1570+95A>C
NM_001185119.1:c.1483+1243A>C	NP_001172048.1:n.1483+1243A>C
NM_018657.4:c.1570+95A>C	NP_061127.1:n.1570+95A>C
NR_033702.1:n.1869+95A>C
NR_033703.1:n.1883+95A>C
XM_005247621.3:c.1486+95A>C	XP_005247678.1:n.1486+95A>C
XM_005247622.3:c.1324+95A>C	XP_005247679.1:n.1324+95A>C
XM_005247624.3:c.1228+95A>C	XP_005247681.1:n.1228+95A>C
XM_011512987.1:c.1570+95A>C	XP_011511289.1:n.1570+95A>C
XM_011512988.1:c.1570+95A>C	XP_011511290.1:n.1570+95A>C
XM_005247621.5:c.1486+95A>C	XP_005247678.1:n.1486+95A>C
XM_005247622.4:c.1324+95A>C	XP_005247679.1:n.1324+95A>C
XM_005247624.4:c.1228+95A>C	XP_005247681.1:n.1228+95A>C
XM_017006864.2:c.1570+95A>C	XP_016862353.1:n.1570+95A>C
XM_017006865.2:c.1144+95A>C	XP_016862354.1:n.1144+95A>C
XM_017006866.2:c.1144+95A>C	XP_016862355.1:n.1144+95A>C
XM_017006867.2:c.751+95A>C	XP_016862356.1:n.751+95A>C
XM_017006868.2:c.667+95A>C	XP_016862357.1:n.667+95A>C
XR_002959552.1:n.3402+95A>C
NM_001185118.2:c.1570+95A>C	NP_001172047.1:n.1570+95A>C
NM_018657.5:c.1570+95A>C MANE Select	NP_061127.1:n.1570+95A>C
NR_033702.2:n.1538+95A>C
NR_033703.2:n.1552+95A>C