Canonical Allele Identifier: CA1845635991
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647401C= , CM000671.2:g.34647401C= GRCh38
NC_000009.11:g.34647398C= , CM000671.1:g.34647398C= GRCh37
NC_000009.10:g.34637398C= NCBI36
NG_009029.1:g.5764C=
NG_028966.1:g.217C=
NG_009029.2:g.5813C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.253-91C= ENSP00000509954.1:n.253-91C=
ENST00000378842.8:c.253-91C= MANE Select ENSP00000368119.4:n.253-91C=
ENST00000378842.7:c.253-91C= ENSP00000368119.3:n.253-91C=
ENST00000450095.6:c.50+143C= ENSP00000401956.2:n.50+143C=
ENST00000465543.6:n.592-91C=
ENST00000468099.2:n.435C=
ENST00000472111.5:n.294-91C=
ENST00000473506.6:c.253-140C= ENSP00000432839.2:n.253-140C=
ENST00000473529.5:n.300-91C=
ENST00000485531.1:n.388C=
ENST00000487381.5:n.421C=
ENST00000489643.6:n.282+143C=
ENST00000554085.5:c.253-74C= ENSP00000450419.1:n.253-74C=
ENST00000554139.5:n.306-91C=
ENST00000554330.5:n.250-140C=
ENST00000554550.5:c.252+143C= ENSP00000451435.1:n.252+143C=
ENST00000554638.5:n.419C=
ENST00000554897.5:c.252+143C= ENSP00000450942.1:n.252+143C=
ENST00000554944.5:n.283-140C=
ENST00000555020.5:n.283-91C=
ENST00000555086.5:n.257-91C=
ENST00000555214.5:n.261+143C=
ENST00000556157.1:n.360-74C=
ENST00000556244.1:c.149C=
ENST00000556278.1:c.252+143C= ENSP00000451792.1:n.252+143C=
ENST00000556403.5:n.266-91C=
ENST00000556494.5:n.285-91C=
ENST00000557541.5:n.446-140C=
ENST00000557706.5:n.509C=
NM_000155.3:c.253-91C= NP_000146.2:n.253-91C=
NM_001258332.1:c.50+143C= NP_001245261.1:n.50+143C=
NM_000155.4:c.253-91C= MANE Select NP_000146.2:n.253-91C=
NM_001258332.2:c.50+143C= NP_001245261.1:n.50+143C=