Canonical Allele Identifier: CA464595870

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647700C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647703C>T , CM000671.2:g.34647703C>T	GRCh38
NC_000009.11:g.34647700C>T , CM000671.1:g.34647700C>T	GRCh37
NC_000009.10:g.34637700C>T	NCBI36
NG_009029.1:g.6066C>T
NG_028966.1:g.519C>T
NG_009029.2:g.6115C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.329-129C>T	ENSP00000509954.1:n.329-129C>T
ENST00000378842.8:c.375C>T MANE Select	ENSP00000368119.4:p.Val125=
ENST00000378842.7:c.375C>T	ENSP00000368119.3:p.Val125=
ENST00000450095.6:c.51-129C>T	ENSP00000401956.2:n.51-129C>T
ENST00000465543.6:n.714C>T
ENST00000472111.5:n.505C>T
ENST00000473506.6:c.326C>T	ENSP00000432839.2:p.Ser109Phe
ENST00000473529.5:n.511C>T
ENST00000485531.1:n.690C>T
ENST00000487381.5:n.634C>T
ENST00000489643.6:n.283-412C>T
ENST00000554085.5:c.*119C>T	ENSP00000450419.1:n.*119C>T
ENST00000554139.5:n.428C>T
ENST00000554330.5:n.412C>T
ENST00000554550.5:c.253-129C>T	ENSP00000451435.1:n.253-129C>T
ENST00000554638.5:n.721C>T
ENST00000554897.5:c.253-129C>T	ENSP00000450942.1:n.253-129C>T
ENST00000554944.5:n.445C>T
ENST00000555020.5:n.405C>T
ENST00000555086.5:n.379C>T
ENST00000555214.5:n.262-345C>T
ENST00000556157.1:n.499C>T
ENST00000556244.1:c.362C>T
ENST00000556278.1:c.253-412C>T	ENSP00000451792.1:n.253-412C>T
ENST00000556403.5:n.477C>T
ENST00000556494.5:n.496C>T
ENST00000557541.5:n.519C>T
ENST00000557706.5:n.811C>T
NM_000155.3:c.375C>T	NP_000146.2:p.Val125=
NM_001258332.1:c.51-129C>T	NP_001245261.1:n.51-129C>T
NM_000155.4:c.375C>T MANE Select	NP_000146.2:p.Val125=
NM_001258332.2:c.51-129C>T	NP_001245261.1:n.51-129C>T