Canonical Allele Identifier: CA2521138976

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973988_141973989insACA , CM000669.2:g.141973988_141973989insACA GRCh38
NC_000007.13:g.141673788_141673789insACA , CM000669.1:g.141673788_141673789insACA GRCh37
NC_000007.12:g.141320257_141320258insACA NCBI36
NG_016141.1:g.4785_4786insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27991_-3+27992insACA (MGAM) ENSP00000419372.1:n.-3+27991_-3+27992insACA
XM_011515783.1:c.*25-12408_*25-12407insACA (OR9A4) XP_011514085.1:n.*25-12408_*25-12407insACA