Canonical Allele Identifier: CA1069116732
Gene: MMAA HGNC NCBI

Linked Data

dbSNP Id: rs1727732408

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145639820_145639821insA , CM000666.2:g.145639820_145639821insA GRCh38
NC_000004.11:g.146560972_146560973insA , CM000666.1:g.146560972_146560973insA GRCh37
NC_000004.10:g.146780422_146780423insA NCBI36
NG_007536.1:g.25523_25524insA
NG_007536.2:g.45779_45780insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000541599.5:c.439+242_439+243insA ENSP00000442284.3:n.439+242_439+243insA
ENST00000647947.1:c.*177_*178insA ENSP00000496781.1:n.*177_*178insA
ENST00000648388.1:c.439+242_439+243insA ENSP00000497046.1:n.439+242_439+243insA
ENST00000649156.2:c.439+242_439+243insA MANE Select ENSP00000497008.1:n.439+242_439+243insA
ENST00000649173.1:c.439+242_439+243insA ENSP00000497871.1:n.439+242_439+243insA
ENST00000649704.1:c.439+242_439+243insA ENSP00000497680.1:n.439+242_439+243insA
ENST00000679563.1:c.439+242_439+243insA ENSP00000506503.1:n.439+242_439+243insA
ENST00000679930.1:c.435+246_435+247insA ENSP00000506293.1:n.435+246_435+247insA
ENST00000281317.9:c.439+242_439+243insA ENSP00000281317.5:n.439+242_439+243insA
ENST00000506919.1:n.927+242_927+243insA
ENST00000511969.4:c.439+242_439+243insA ENSP00000427422.1:n.439+242_439+243insA
ENST00000541599.4:c.439+242_439+243insA ENSP00000442284.2:n.439+242_439+243insA
NM_172250.2:c.439+242_439+243insA NP_758454.1:n.439+242_439+243insA
XM_011531684.1:c.439+242_439+243insA XP_011529986.1:n.439+242_439+243insA
XM_011531685.1:c.439+242_439+243insA XP_011529987.1:n.439+242_439+243insA
XM_011531686.1:c.-103_-102insA XP_011529988.1:n.-103_-102insA
NM_172250.3:c.439+242_439+243insA MANE Select NP_758454.1:n.439+242_439+243insA
XM_011531684.3:c.439+242_439+243insA XP_011529986.1:n.439+242_439+243insA
XM_011531685.2:c.439+242_439+243insA XP_011529987.1:n.439+242_439+243insA
XM_011531686.2:c.-103_-102insA XP_011529988.1:n.-103_-102insA
NM_001375644.1:c.439+242_439+243insA NP_001362573.1:n.439+242_439+243insA