Canonical Allele Identifier: CA1845635428
Community Standard Title: NM_000155.4(GALT):c.134C= (p.Ser45=)
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647140C= , CM000671.2:g.34647140C= GRCh38
NC_000009.11:g.34647137C= , CM000671.1:g.34647137C= GRCh37
NC_000009.10:g.34637137C= NCBI36
NG_009029.1:g.5503C=
NG_009029.2:g.5552C=

Transcript Alleles

HGVS Amino-acid Change
NM_000155.4:c.134C= MANE Select NP_000146.2:p.Ser45=
ENST00000378842.8:c.134C= MANE Select ENSP00000368119.4:p.Ser45=
NM_000155.3:c.134C= NP_000146.2:p.Ser45=
NM_001258332.1:c.-69C= NP_001245261.1:n.-69C=
NM_001258332.2:c.-69C= NP_001245261.1:n.-69C=
ENST00000378842.7:c.134C= ENSP00000368119.3:p.Ser45=
ENST00000450095.6:c.-69C= ENSP00000401956.2:n.-69C=
ENST00000465543.6:n.473C=
ENST00000468099.2:n.174C=
ENST00000472111.5:n.175C=
ENST00000473506.6:c.134C= ENSP00000432839.2:p.Ser45=
ENST00000473529.5:n.181C=
ENST00000485531.1:n.127C=
ENST00000487381.5:n.160C=
ENST00000489643.6:n.164C=
ENST00000554085.5:c.134C= ENSP00000450419.1:p.Ser45=
ENST00000554139.5:n.187C=
ENST00000554330.5:n.131C=
ENST00000554550.5:c.134C= ENSP00000451435.1:p.Ser45=
ENST00000554638.5:n.158C=
ENST00000554897.5:c.134C= ENSP00000450942.1:p.Ser45=
ENST00000554944.5:n.164C=
ENST00000555020.5:n.164C=
ENST00000555086.5:n.138C=
ENST00000555214.5:n.143C=
ENST00000556157.1:n.241C=
ENST00000556244.1:c.18C=
ENST00000556278.1:c.134C= ENSP00000451792.1:p.Ser45=
ENST00000556403.5:n.147C=
ENST00000556494.5:n.166C=
ENST00000557541.5:n.327C=
ENST00000557706.5:n.248C=
ENST00000605275.1:n.672C=
ENST00000691183.1:c.134C= ENSP00000509954.1:p.Ser45=