Canonical Allele Identifier: CA1845636495
Community Standard Title: NM_000155.4(GALT):c.334A= (p.Ser112=)
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647662A= , CM000671.2:g.34647662A= GRCh38
NC_000009.11:g.34647659A= , CM000671.1:g.34647659A= GRCh37
NC_000009.10:g.34637659A= NCBI36
NG_009029.1:g.6025A=
NG_028966.1:g.478A=
NG_009029.2:g.6074A=

Transcript Alleles

HGVS Amino-acid Change
NM_000155.4:c.334A= MANE Select NP_000146.2:p.Ser112=
ENST00000378842.8:c.334A= MANE Select ENSP00000368119.4:p.Ser112=
NM_000155.3:c.334A= NP_000146.2:p.Ser112=
NM_001258332.1:c.51-170A= NP_001245261.1:n.51-170A=
NM_001258332.2:c.51-170A= NP_001245261.1:n.51-170A=
ENST00000378842.7:c.334A= ENSP00000368119.3:p.Ser112=
ENST00000450095.6:c.51-170A= ENSP00000401956.2:n.51-170A=
ENST00000465543.6:n.673A=
ENST00000472111.5:n.464A=
ENST00000473506.6:c.285A= ENSP00000432839.2:p.Pro95=
ENST00000473529.5:n.470A=
ENST00000485531.1:n.649A=
ENST00000487381.5:n.593A=
ENST00000489643.6:n.282+404A=
ENST00000554085.5:c.*78A= ENSP00000450419.1:n.*78A=
ENST00000554139.5:n.387A=
ENST00000554330.5:n.371A=
ENST00000554550.5:c.253-170A= ENSP00000451435.1:n.253-170A=
ENST00000554638.5:n.680A=
ENST00000554897.5:c.253-170A= ENSP00000450942.1:n.253-170A=
ENST00000554944.5:n.404A=
ENST00000555020.5:n.364A=
ENST00000555086.5:n.338A=
ENST00000555214.5:n.262-386A=
ENST00000556157.1:n.458A=
ENST00000556244.1:c.321A=
ENST00000556278.1:c.252+404A= ENSP00000451792.1:n.252+404A=
ENST00000556403.5:n.436A=
ENST00000556494.5:n.455A=
ENST00000557541.5:n.478A=
ENST00000557706.5:n.770A=
ENST00000691183.1:c.328+95A= ENSP00000509954.1:n.328+95A=