Canonical Allele Identifier: CA45602339
Gene: GALM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38681143dup , CM000664.2:g.38681143dup GRCh38
NC_000002.11:g.38908285dup , CM000664.1:g.38908285dup GRCh37
NC_000002.10:g.38761789dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272252.10:c.346-137dup MANE Select ENSP00000272252.5:n.346-137dup
ENST00000272252.9:c.346-137dup ENSP00000272252.5:n.346-137dup
ENST00000410063.5:c.190+14792dup ENSP00000386233.1:n.190+14792dup
ENST00000427858.4:n.529-137dup
ENST00000444351.5:c.265-137dup ENSP00000409083.1:n.265-137dup
NM_138801.2:c.346-137dup NP_620156.1:n.346-137dup
XM_011532540.1:c.346-137dup XP_011530842.1:n.346-137dup
XR_244925.1:n.598-137dup
XM_011532540.2:c.346-137dup XP_011530842.1:n.346-137dup
XR_244925.2:n.586-137dup
NM_138801.3:c.346-137dup MANE Select NP_620156.1:n.346-137dup