Canonical Allele Identifier: CA1845638573
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648344G= , CM000671.2:g.34648344G= GRCh38
NC_000009.11:g.34648341G= , CM000671.1:g.34648341G= GRCh37
NC_000009.10:g.34638341G= NCBI36
NG_009029.1:g.6707G=
NG_028966.1:g.1160G=
NG_009029.2:g.6756G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.*163G= ENSP00000509954.1:n.*163G=
ENST00000378842.8:c.575G= MANE Select ENSP00000368119.4:p.Ser192=
ENST00000378842.7:c.575G= ENSP00000368119.3:p.Ser192=
ENST00000450095.6:c.248G= ENSP00000401956.2:p.Ser83=
ENST00000472111.5:n.831G=
ENST00000473506.6:c.*163G= ENSP00000432839.2:n.*163G=
ENST00000473529.5:n.734G=
ENST00000485531.1:n.1169G=
ENST00000487381.5:n.960G=
ENST00000489643.6:n.350G=
ENST00000554085.5:c.*319G= ENSP00000450419.1:n.*319G=
ENST00000554139.5:n.821G=
ENST00000554550.5:c.*195G= ENSP00000451435.1:n.*195G=
ENST00000554638.5:n.1047G=
ENST00000554897.5:c.*262G= ENSP00000450942.1:n.*262G=
ENST00000554944.5:n.924G=
ENST00000555020.5:n.731G=
ENST00000555086.5:n.579G=
ENST00000555214.5:n.396G=
ENST00000556244.1:c.562G=
ENST00000556278.1:c.320G= ENSP00000451792.1:p.Ser107=
ENST00000556494.5:n.696G=
ENST00000557706.5:n.1137G=
NM_000155.3:c.575G= NP_000146.2:p.Ser192=
NM_001258332.1:c.248G= NP_001245261.1:p.Ser83=
NM_000155.4:c.575G= MANE Select NP_000146.2:p.Ser192=
NM_001258332.2:c.248G= NP_001245261.1:p.Ser83=