Canonical Allele Identifier: CA1845636623

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647705G= , CM000671.2:g.34647705G=	GRCh38
NC_000009.11:g.34647702G= , CM000671.1:g.34647702G=	GRCh37
NC_000009.10:g.34637702G=	NCBI36
NG_009029.1:g.6068G=
NG_028966.1:g.521G=
NG_009029.2:g.6117G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.329-127G=	ENSP00000509954.1:n.329-127G=
ENST00000378842.8:c.377G= MANE Select	ENSP00000368119.4:p.Cys126=
ENST00000378842.7:c.377G=	ENSP00000368119.3:p.Cys126=
ENST00000450095.6:c.51-127G=	ENSP00000401956.2:n.51-127G=
ENST00000465543.6:n.716G=
ENST00000472111.5:n.507G=
ENST00000473506.6:c.328G=	ENSP00000432839.2:p.Val110=
ENST00000473529.5:n.513G=
ENST00000485531.1:n.692G=
ENST00000487381.5:n.636G=
ENST00000489643.6:n.283-410G=
ENST00000554085.5:c.*121G=	ENSP00000450419.1:n.*121G=
ENST00000554139.5:n.430G=
ENST00000554330.5:n.414G=
ENST00000554550.5:c.253-127G=	ENSP00000451435.1:n.253-127G=
ENST00000554638.5:n.723G=
ENST00000554897.5:c.253-127G=	ENSP00000450942.1:n.253-127G=
ENST00000554944.5:n.447G=
ENST00000555020.5:n.407G=
ENST00000555086.5:n.381G=
ENST00000555214.5:n.262-343G=
ENST00000556157.1:n.501G=
ENST00000556244.1:c.364G=
ENST00000556278.1:c.253-410G=	ENSP00000451792.1:n.253-410G=
ENST00000556403.5:n.479G=
ENST00000556494.5:n.498G=
ENST00000557541.5:n.521G=
ENST00000557706.5:n.813G=
NM_000155.3:c.377G=	NP_000146.2:p.Cys126=
NM_001258332.1:c.51-127G=	NP_001245261.1:n.51-127G=
NM_000155.4:c.377G= MANE Select	NP_000146.2:p.Cys126=
NM_001258332.2:c.51-127G=	NP_001245261.1:n.51-127G=