Canonical Allele Identifier: CA464595698
Gene: GALT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.34647138A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647141A>C , CM000671.2:g.34647141A>C GRCh38
NC_000009.11:g.34647138A>C , CM000671.1:g.34647138A>C GRCh37
NC_000009.10:g.34637138A>C NCBI36
NG_009029.1:g.5504A>C
NG_009029.2:g.5553A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.135A>C ENSP00000509954.1:p.Ser45=
ENST00000378842.8:c.135A>C MANE Select ENSP00000368119.4:p.Ser45=
ENST00000378842.7:c.135A>C ENSP00000368119.3:p.Ser45=
ENST00000450095.6:c.-68A>C ENSP00000401956.2:n.-68A>C
ENST00000465543.6:n.474A>C
ENST00000468099.2:n.175A>C
ENST00000472111.5:n.176A>C
ENST00000473506.6:c.135A>C ENSP00000432839.2:p.Ser45=
ENST00000473529.5:n.182A>C
ENST00000485531.1:n.128A>C
ENST00000487381.5:n.161A>C
ENST00000489643.6:n.165A>C
ENST00000554085.5:c.135A>C ENSP00000450419.1:p.Ser45=
ENST00000554139.5:n.188A>C
ENST00000554330.5:n.132A>C
ENST00000554550.5:c.135A>C ENSP00000451435.1:p.Ser45=
ENST00000554638.5:n.159A>C
ENST00000554897.5:c.135A>C ENSP00000450942.1:p.Ser45=
ENST00000554944.5:n.165A>C
ENST00000555020.5:n.165A>C
ENST00000555086.5:n.139A>C
ENST00000555214.5:n.144A>C
ENST00000556157.1:n.242A>C
ENST00000556244.1:c.19A>C
ENST00000556278.1:c.135A>C ENSP00000451792.1:p.Ser45=
ENST00000556403.5:n.148A>C
ENST00000556494.5:n.167A>C
ENST00000557541.5:n.328A>C
ENST00000557706.5:n.249A>C
ENST00000605275.1:n.673A>C
NM_000155.3:c.135A>C NP_000146.2:p.Ser45=
NM_001258332.1:c.-68A>C NP_001245261.1:n.-68A>C
NM_000155.4:c.135A>C MANE Select NP_000146.2:p.Ser45=
NM_001258332.2:c.-68A>C NP_001245261.1:n.-68A>C