Canonical Allele Identifier: CA6663802

Gene: MON2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.62546899G>A , CM000674.2:g.62546899G>A	GRCh38
NC_000012.11:g.62940679G>A , CM000674.1:g.62940679G>A	GRCh37
NC_000012.10:g.61226946G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393630.8:c.2580G>A MANE Select	ENSP00000377250.4:p.Arg860=
ENST00000641654.1:c.2583G>A	ENSP00000493462.1:p.Arg861=
ENST00000393629.6:c.2580G>A	ENSP00000377249.2:p.Arg860=
ENST00000393630.7:c.2580G>A	ENSP00000377250.4:p.Arg860=
ENST00000546600.5:c.2580G>A	ENSP00000447407.1:p.Arg860=
ENST00000547095.5:c.*2526G>A	ENSP00000446626.1:n.*2526G>A
ENST00000552115.5:c.2580G>A	ENSP00000446635.1:p.Arg860=
ENST00000552738.5:c.2511G>A	ENSP00000449215.1:p.Arg837=
NM_001278469.1:c.2580G>A	NP_001265398.1:p.Arg860=
NM_001278470.1:c.2580G>A	NP_001265399.1:p.Arg860=
NM_001278471.1:c.2511G>A	NP_001265400.1:p.Arg837=
NM_001278472.1:c.2364G>A	NP_001265401.1:p.Arg788=
NM_015026.2:c.2580G>A	NP_055841.2:p.Arg860=
XM_011538051.1:c.2364G>A	XP_011536353.1:p.Arg788=
XM_011538052.1:c.2580G>A	XP_011536354.1:p.Arg860=
XR_944510.1:n.2971G>A
NM_001278469.2:c.2580G>A	NP_001265398.1:p.Arg860=
XM_017019041.1:c.2583G>A	XP_016874530.1:p.Arg861=
XM_017019042.1:c.2583G>A	XP_016874531.1:p.Arg861=
XM_017019043.1:c.2367G>A	XP_016874532.1:p.Arg789=
XM_017019044.1:c.2367G>A	XP_016874533.1:p.Arg789=
XM_017019045.1:c.2367G>A	XP_016874534.1:p.Arg789=
XM_017019046.1:c.915G>A	XP_016874535.1:p.Arg305=
XR_001748627.1:n.2974G>A
XR_001748628.1:n.2974G>A
XR_001748629.1:n.2974G>A
NM_015026.3:c.2580G>A MANE Select	NP_055841.2:p.Arg860=
NM_001278469.3:c.2580G>A	NP_001265398.1:p.Arg860=
NM_001278470.2:c.2580G>A	NP_001265399.1:p.Arg860=
NM_001278471.2:c.2511G>A	NP_001265400.1:p.Arg837=
NM_001278472.2:c.2364G>A	NP_001265401.1:p.Arg788=