Canonical Allele Identifier: CA1845640956
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34649355C= , CM000671.2:g.34649355C= GRCh38
NC_000009.11:g.34649352C= , CM000671.1:g.34649352C= GRCh37
NC_000009.10:g.34639352C= NCBI36
NG_009029.1:g.7718C=
NG_028966.1:g.2171C=
NG_009029.2:g.7767C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*493-55C= ENSP00000509954.1:n.*493-55C=
ENST00000378842.8:c.905-55C= MANE Select ENSP00000368119.4:n.905-55C=
ENST00000378842.7:c.905-55C= ENSP00000368119.3:n.905-55C=
ENST00000450095.6:c.578-55C= ENSP00000401956.2:n.578-55C=
ENST00000488412.2:n.434C=
ENST00000489643.6:n.1258C=
ENST00000554550.5:c.*525-55C= ENSP00000451435.1:n.*525-55C=
ENST00000554638.5:n.1377-55C=
ENST00000555020.5:n.1639C=
ENST00000555754.1:n.353-55C=
ENST00000556278.1:c.432+899C= ENSP00000451792.1:n.432+899C=
ENST00000557706.5:n.1480-55C=
NM_000155.3:c.905-55C= NP_000146.2:n.905-55C=
NM_001258332.1:c.578-55C= NP_001245261.1:n.578-55C=
NM_000155.4:c.905-55C= MANE Select NP_000146.2:n.905-55C=
NM_001258332.2:c.578-55C= NP_001245261.1:n.578-55C=