Canonical Allele Identifier: CA1501192468
Gene: MMAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145639280T= , CM000666.2:g.145639280T= GRCh38
NC_000004.11:g.146560432T= , CM000666.1:g.146560432T= GRCh37
NC_000004.10:g.146779882T= NCBI36
NG_007536.1:g.24983T=
NG_007536.2:g.45239T=

Transcript Alleles

HGVS Amino-acid change
ENST00000541599.5:c.141T= ENSP00000442284.3:p.Leu47=
ENST00000647947.1:c.141T= ENSP00000496781.1:p.Leu47=
ENST00000648388.1:c.141T= ENSP00000497046.1:p.Leu47=
ENST00000649156.2:c.141T= MANE Select ENSP00000497008.1:p.Leu47=
ENST00000649173.1:c.141T= ENSP00000497871.1:p.Leu47=
ENST00000649704.1:c.141T= ENSP00000497680.1:p.Leu47=
ENST00000679563.1:c.141T= ENSP00000506503.1:p.Leu47=
ENST00000679930.1:c.141T= ENSP00000506293.1:p.Leu47=
ENST00000281317.9:c.141T= ENSP00000281317.5:p.Leu47=
ENST00000506919.1:n.629T=
ENST00000511969.4:c.141T= ENSP00000427422.1:p.Leu47=
ENST00000541599.4:c.141T= ENSP00000442284.2:p.Leu47=
NM_172250.2:c.141T= NP_758454.1:p.Leu47=
XM_011531684.1:c.141T= XP_011529986.1:p.Leu47=
XM_011531685.1:c.141T= XP_011529987.1:p.Leu47=
NM_172250.3:c.141T= MANE Select NP_758454.1:p.Leu47=
XM_011531684.3:c.141T= XP_011529986.1:p.Leu47=
XM_011531685.2:c.141T= XP_011529987.1:p.Leu47=
XM_011531686.2:c.-643T= XP_011529988.1:n.-643T=
NM_001375644.1:c.141T= NP_001362573.1:p.Leu47=