Canonical Allele Identifier: CA1845636667

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647712A= , CM000671.2:g.34647712A=	GRCh38
NC_000009.11:g.34647709A= , CM000671.1:g.34647709A=	GRCh37
NC_000009.10:g.34637709A=	NCBI36
NG_009029.1:g.6075A=
NG_028966.1:g.528A=
NG_009029.2:g.6124A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.329-120A=	ENSP00000509954.1:n.329-120A=
ENST00000378842.8:c.377+7A= MANE Select	ENSP00000368119.4:n.377+7A=
ENST00000378842.7:c.377+7A=	ENSP00000368119.3:n.377+7A=
ENST00000450095.6:c.51-120A=	ENSP00000401956.2:n.51-120A=
ENST00000465543.6:n.716+7A=
ENST00000472111.5:n.514A=
ENST00000473506.6:c.328+7A=	ENSP00000432839.2:n.328+7A=
ENST00000473529.5:n.513+7A=
ENST00000485531.1:n.699A=
ENST00000487381.5:n.643A=
ENST00000489643.6:n.283-403A=
ENST00000554085.5:c.*121+7A=	ENSP00000450419.1:n.*121+7A=
ENST00000554139.5:n.437A=
ENST00000554330.5:n.421A=
ENST00000554550.5:c.253-120A=	ENSP00000451435.1:n.253-120A=
ENST00000554638.5:n.730A=
ENST00000554897.5:c.253-120A=	ENSP00000450942.1:n.253-120A=
ENST00000554944.5:n.454A=
ENST00000555020.5:n.414A=
ENST00000555086.5:n.381+7A=
ENST00000555214.5:n.262-336A=
ENST00000556157.1:n.508A=
ENST00000556244.1:c.364+7A=
ENST00000556278.1:c.253-403A=	ENSP00000451792.1:n.253-403A=
ENST00000556403.5:n.486A=
ENST00000556494.5:n.498+7A=
ENST00000557541.5:n.521+7A=
ENST00000557706.5:n.820A=
NM_000155.3:c.377+7A=	NP_000146.2:n.377+7A=
NM_001258332.1:c.51-120A=	NP_001245261.1:n.51-120A=
NM_000155.4:c.377+7A= MANE Select	NP_000146.2:n.377+7A=
NM_001258332.2:c.51-120A=	NP_001245261.1:n.51-120A=