Canonical Allele Identifier: CA441717452
Gene: MMAA HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.146576337T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145655185T>A , CM000666.2:g.145655185T>A GRCh38
NC_000004.11:g.146576337T>A , CM000666.1:g.146576337T>A GRCh37
NC_000004.10:g.146795787T>A NCBI36
NG_007536.1:g.40888T>A
NG_007536.2:g.61144T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000541599.5:c.1008T>A ENSP00000442284.3:p.Ser336=
ENST00000647947.1:c.*792T>A ENSP00000496781.1:n.*792T>A
ENST00000648388.1:c.1008T>A ENSP00000497046.1:p.Ser336=
ENST00000649156.2:c.1008T>A MANE Select ENSP00000497008.1:p.Ser336=
ENST00000649173.1:c.942T>A ENSP00000497871.1:p.Ser314=
ENST00000649704.1:c.1008T>A ENSP00000497680.1:p.Ser336=
ENST00000679563.1:c.1008T>A ENSP00000506503.1:p.Ser336=
ENST00000679930.1:c.*527T>A ENSP00000506293.1:n.*527T>A
ENST00000281317.9:c.1008T>A ENSP00000281317.5:p.Ser336=
ENST00000503730.1:n.418T>A
ENST00000511969.4:c.*139T>A ENSP00000427422.1:n.*139T>A
ENST00000541599.4:c.1008T>A ENSP00000442284.2:p.Ser336=
NM_172250.2:c.1008T>A NP_758454.1:p.Ser336=
XM_011531684.1:c.1008T>A XP_011529986.1:p.Ser336=
XM_011531685.1:c.1008T>A XP_011529987.1:p.Ser336=
XM_011531686.1:c.513T>A XP_011529988.1:p.Ser171=
NM_172250.3:c.1008T>A MANE Select NP_758454.1:p.Ser336=
XM_011531684.3:c.1008T>A XP_011529986.1:p.Ser336=
XM_011531685.2:c.1008T>A XP_011529987.1:p.Ser336=
XM_011531686.2:c.513T>A XP_011529988.1:p.Ser171=
NM_001375644.1:c.1008T>A NP_001362573.1:p.Ser336=