Canonical Allele Identifier: CA1501193444

Gene: MMAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145639871_145639872delinsGT , CM000666.2:g.145639871_145639872delinsGT	GRCh38
NC_000004.11:g.146561023_146561024delinsGT , CM000666.1:g.146561023_146561024delinsGT	GRCh37
NC_000004.10:g.146780473_146780474delinsGT	NCBI36
NG_007536.1:g.25574_25575delinsGT
NG_007536.2:g.45830_45831delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541599.5:c.439+293_439+294delinsGT	ENSP00000442284.3:n.439+293_439+294delinsGT
ENST00000647947.1:c.*223+5_*223+6delinsGT	ENSP00000496781.1:n.*223+5_*223+6delinsGT
ENST00000648388.1:c.439+293_439+294delinsGT	ENSP00000497046.1:n.439+293_439+294delinsGT
ENST00000649156.2:c.439+293_439+294delinsGT MANE Select	ENSP00000497008.1:n.439+293_439+294delinsGT
ENST00000649173.1:c.439+293_439+294delinsGT	ENSP00000497871.1:n.439+293_439+294delinsGT
ENST00000649704.1:c.439+293_439+294delinsGT	ENSP00000497680.1:n.439+293_439+294delinsGT
ENST00000679563.1:c.439+293_439+294delinsGT	ENSP00000506503.1:n.439+293_439+294delinsGT
ENST00000679930.1:c.435+297_435+298delinsGT	ENSP00000506293.1:n.435+297_435+298delinsGT
ENST00000281317.9:c.439+293_439+294delinsGT	ENSP00000281317.5:n.439+293_439+294delinsGT
ENST00000506919.1:n.927+293_927+294delinsGT
ENST00000511969.4:c.439+293_439+294delinsGT	ENSP00000427422.1:n.439+293_439+294delinsGT
ENST00000541599.4:c.439+293_439+294delinsGT	ENSP00000442284.2:n.439+293_439+294delinsGT
NM_172250.2:c.439+293_439+294delinsGT	NP_758454.1:n.439+293_439+294delinsGT
XM_011531684.1:c.439+293_439+294delinsGT	XP_011529986.1:n.439+293_439+294delinsGT
XM_011531685.1:c.439+293_439+294delinsGT	XP_011529987.1:n.439+293_439+294delinsGT
XM_011531686.1:c.-57+5_-57+6delinsGT	XP_011529988.1:n.-57+5_-57+6delinsGT
NM_172250.3:c.439+293_439+294delinsGT MANE Select	NP_758454.1:n.439+293_439+294delinsGT
XM_011531684.3:c.439+293_439+294delinsGT	XP_011529986.1:n.439+293_439+294delinsGT
XM_011531685.2:c.439+293_439+294delinsGT	XP_011529987.1:n.439+293_439+294delinsGT
XM_011531686.2:c.-57+5_-57+6delinsGT	XP_011529988.1:n.-57+5_-57+6delinsGT
NM_001375644.1:c.439+293_439+294delinsGT	NP_001362573.1:n.439+293_439+294delinsGT