Canonical Allele Identifier: CA355057333

Gene: MYNN

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169774313C>G , CM000665.2:g.169774313C>G	GRCh38
NC_000003.11:g.169492101C>G , CM000665.1:g.169492101C>G	GRCh37
NC_000003.10:g.170974795C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.18C>G MANE Select	ENSP00000326240.4:p.His6Gln
ENST00000349841.9:c.18C>G	ENSP00000326240.4:p.His6Gln
ENST00000356716.8:c.18C>G	ENSP00000349150.3:p.His6Gln
ENST00000544106.5:c.18C>G	ENSP00000440637.1:p.His6Gln
ENST00000602751.5:c.18C>G	ENSP00000473654.1:p.His6Gln
NM_001185118.1:c.18C>G	NP_001172047.1:p.His6Gln
NM_001185119.1:c.18C>G	NP_001172048.1:p.His6Gln
NM_018657.4:c.18C>G	NP_061127.1:p.His6Gln
NR_033702.1:n.447C>G
NR_033703.1:n.447C>G
XM_005247621.3:c.18C>G	XP_005247678.1:p.His6Gln
XM_005247622.3:c.18C>G	XP_005247679.1:p.His6Gln
XM_005247624.3:c.-195C>G	XP_005247681.1:n.-195C>G
XM_011512987.1:c.18C>G	XP_011511289.1:p.His6Gln
XM_011512988.1:c.18C>G	XP_011511290.1:p.His6Gln
XM_005247621.5:c.18C>G	XP_005247678.1:p.His6Gln
XM_005247622.4:c.18C>G	XP_005247679.1:p.His6Gln
XM_005247624.4:c.-195C>G	XP_005247681.1:n.-195C>G
XM_017006864.2:c.18C>G	XP_016862353.1:p.His6Gln
XM_017006865.2:c.-195C>G	XP_016862354.1:n.-195C>G
XM_017006866.2:c.-195C>G	XP_016862355.1:n.-195C>G
XM_017006867.2:c.-686C>G	XP_016862356.1:n.-686C>G
XM_017006868.2:c.-686C>G	XP_016862357.1:n.-686C>G
XR_002959552.1:n.719C>G
NM_001185118.2:c.18C>G	NP_001172047.1:p.His6Gln
NM_018657.5:c.18C>G MANE Select	NP_061127.1:p.His6Gln
NR_033702.2:n.116C>G
NR_033703.2:n.116C>G