Canonical Allele Identifier: CA788579048
Gene: MMAA HGNC NCBI

Linked Data

dbSNP Id: rs1173600324

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145639736_145639738del , CM000666.2:g.145639736_145639738del GRCh38
NC_000004.11:g.146560888_146560890del , CM000666.1:g.146560888_146560890del GRCh37
NC_000004.10:g.146780338_146780340del NCBI36
NG_007536.1:g.25439_25441del
NG_007536.2:g.45695_45697del

Transcript Alleles

HGVS Amino-acid Change
ENST00000541599.5:c.439+158_439+160del ENSP00000442284.3:n.439+158_439+160del
ENST00000647947.1:c.*93_*95del ENSP00000496781.1:n.*93_*95del
ENST00000648388.1:c.439+158_439+160del ENSP00000497046.1:n.439+158_439+160del
ENST00000649156.2:c.439+158_439+160del MANE Select ENSP00000497008.1:n.439+158_439+160del
ENST00000649173.1:c.439+158_439+160del ENSP00000497871.1:n.439+158_439+160del
ENST00000649704.1:c.439+158_439+160del ENSP00000497680.1:n.439+158_439+160del
ENST00000679563.1:c.439+158_439+160del ENSP00000506503.1:n.439+158_439+160del
ENST00000679930.1:c.435+162_435+164del ENSP00000506293.1:n.435+162_435+164del
ENST00000281317.9:c.439+158_439+160del ENSP00000281317.5:n.439+158_439+160del
ENST00000506919.1:n.927+158_927+160del
ENST00000511969.4:c.439+158_439+160del ENSP00000427422.1:n.439+158_439+160del
ENST00000541599.4:c.439+158_439+160del ENSP00000442284.2:n.439+158_439+160del
NM_172250.2:c.439+158_439+160del NP_758454.1:n.439+158_439+160del
XM_011531684.1:c.439+158_439+160del XP_011529986.1:n.439+158_439+160del
XM_011531685.1:c.439+158_439+160del XP_011529987.1:n.439+158_439+160del
XM_011531686.1:c.-187_-185del XP_011529988.1:n.-187_-185del
NM_172250.3:c.439+158_439+160del MANE Select NP_758454.1:n.439+158_439+160del
XM_011531684.3:c.439+158_439+160del XP_011529986.1:n.439+158_439+160del
XM_011531685.2:c.439+158_439+160del XP_011529987.1:n.439+158_439+160del
XM_011531686.2:c.-187_-185del XP_011529988.1:n.-187_-185del
NM_001375644.1:c.439+158_439+160del NP_001362573.1:n.439+158_439+160del