Canonical Allele Identifier: CA1845641422
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34649491C= , CM000671.2:g.34649491C= GRCh38
NC_000009.11:g.34649488C= , CM000671.1:g.34649488C= GRCh37
NC_000009.10:g.34639488C= NCBI36
NG_009029.1:g.7854C=
NG_028966.1:g.2307C=
NG_009029.2:g.7903C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*574C= ENSP00000509954.1:n.*574C=
ENST00000378842.8:c.986C= MANE Select ENSP00000368119.4:p.Ser329=
ENST00000378842.7:c.986C= ENSP00000368119.3:p.Ser329=
ENST00000450095.6:c.659C= ENSP00000401956.2:p.Ser220=
ENST00000488412.2:n.570C=
ENST00000489643.6:n.1394C=
ENST00000554550.5:c.*606C= ENSP00000451435.1:n.*606C=
ENST00000554638.5:n.1458C=
ENST00000555020.5:n.1775C=
ENST00000555754.1:n.434C=
ENST00000556278.1:c.432+1035C= ENSP00000451792.1:n.432+1035C=
ENST00000557706.5:n.1561C=
NM_000155.3:c.986C= NP_000146.2:p.Ser329=
NM_001258332.1:c.659C= NP_001245261.1:p.Ser220=
NM_000155.4:c.986C= MANE Select NP_000146.2:p.Ser329=
NM_001258332.2:c.659C= NP_001245261.1:p.Ser220=