Canonical Allele Identifier: CA107720540
Gene: MMAA HGNC NCBI

Linked Data

dbSNP Id: rs993358804

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145639638T>C , CM000666.2:g.145639638T>C GRCh38
NC_000004.11:g.146560790T>C , CM000666.1:g.146560790T>C GRCh37
NC_000004.10:g.146780240T>C NCBI36
NG_007536.1:g.25341T>C
NG_007536.2:g.45597T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000541599.5:c.439+60T>C ENSP00000442284.3:n.439+60T>C
ENST00000647947.1:c.499T>C ENSP00000496781.1:p.Phe167Leu
ENST00000648388.1:c.439+60T>C ENSP00000497046.1:n.439+60T>C
ENST00000649156.2:c.439+60T>C MANE Select ENSP00000497008.1:n.439+60T>C
ENST00000649173.1:c.439+60T>C ENSP00000497871.1:n.439+60T>C
ENST00000649704.1:c.439+60T>C ENSP00000497680.1:n.439+60T>C
ENST00000679563.1:c.439+60T>C ENSP00000506503.1:n.439+60T>C
ENST00000679930.1:c.435+64T>C ENSP00000506293.1:n.435+64T>C
ENST00000281317.9:c.439+60T>C ENSP00000281317.5:n.439+60T>C
ENST00000506919.1:n.927+60T>C
ENST00000511969.4:c.439+60T>C ENSP00000427422.1:n.439+60T>C
ENST00000541599.4:c.439+60T>C ENSP00000442284.2:n.439+60T>C
NM_172250.2:c.439+60T>C NP_758454.1:n.439+60T>C
XM_011531684.1:c.439+60T>C XP_011529986.1:n.439+60T>C
XM_011531685.1:c.439+60T>C XP_011529987.1:n.439+60T>C
XM_011531686.1:c.-285T>C XP_011529988.1:n.-285T>C
NM_172250.3:c.439+60T>C MANE Select NP_758454.1:n.439+60T>C
XM_011531684.3:c.439+60T>C XP_011529986.1:n.439+60T>C
XM_011531685.2:c.439+60T>C XP_011529987.1:n.439+60T>C
XM_011531686.2:c.-285T>C XP_011529988.1:n.-285T>C
NM_001375644.1:c.439+60T>C NP_001362573.1:n.439+60T>C