Canonical Allele Identifier: CA1501207362
Gene: MMAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145655261C= , CM000666.2:g.145655261C= GRCh38
NC_000004.11:g.146576413C= , CM000666.1:g.146576413C= GRCh37
NC_000004.10:g.146795863C= NCBI36
NG_007536.1:g.40964C=
NG_007536.2:g.61220C=

Transcript Alleles

HGVS Amino-acid change
ENST00000541599.5:c.1084C= ENSP00000442284.3:p.Gln362=
ENST00000647947.1:c.*868C= ENSP00000496781.1:n.*868C=
ENST00000648388.1:c.1084C= ENSP00000497046.1:p.Gln362=
ENST00000649156.2:c.1084C= MANE Select ENSP00000497008.1:p.Gln362=
ENST00000649173.1:c.1018C= ENSP00000497871.1:p.Gln340=
ENST00000649704.1:c.1084C= ENSP00000497680.1:p.Gln362=
ENST00000679563.1:c.1084C= ENSP00000506503.1:p.Gln362=
ENST00000679930.1:c.*603C= ENSP00000506293.1:n.*603C=
ENST00000281317.9:c.1084C= ENSP00000281317.5:p.Gln362=
ENST00000503730.1:n.494C=
ENST00000511969.4:c.*215C= ENSP00000427422.1:n.*215C=
ENST00000541599.4:c.1084C= ENSP00000442284.2:p.Gln362=
NM_172250.2:c.1084C= NP_758454.1:p.Gln362=
XM_011531684.1:c.1084C= XP_011529986.1:p.Gln362=
XM_011531685.1:c.1084C= XP_011529987.1:p.Gln362=
XM_011531686.1:c.589C= XP_011529988.1:p.Gln197=
NM_172250.3:c.1084C= MANE Select NP_758454.1:p.Gln362=
XM_011531684.3:c.1084C= XP_011529986.1:p.Gln362=
XM_011531685.2:c.1084C= XP_011529987.1:p.Gln362=
XM_011531686.2:c.589C= XP_011529988.1:p.Gln197=
NM_001375644.1:c.1084C= NP_001362573.1:p.Gln362=