Canonical Allele Identifier: CA15165224
Community Standard Title: NM_138801.3(GALM):c.776+108A>G
Gene: GALM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38729805A>G , CM000664.2:g.38729805A>G GRCh38
NC_000002.11:g.38956947A>G , CM000664.1:g.38956947A>G GRCh37
NC_000002.10:g.38810451A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_138801.3:c.776+108A>G MANE Select NP_620156.1:n.776+108A>G
ENST00000272252.10:c.776+108A>G MANE Select ENSP00000272252.5:n.776+108A>G
NM_138801.2:c.776+108A>G NP_620156.1:n.776+108A>G
ENST00000272252.9:c.776+108A>G ENSP00000272252.5:n.776+108A>G
ENST00000410063.5:c.332+108A>G ENSP00000386233.1:n.332+108A>G
ENST00000434934.1:c.416+108A>G ENSP00000399473.1:n.416+108A>G
ENST00000444351.5:c.766+108A>G ENSP00000409083.1:n.766+108A>G
XR_244925.1:n.1099+108A>G
XR_244925.2:n.1087+108A>G
XR_939976.1:n.85+3661T>C