Canonical Allele Identifier: CA1845639663

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648818A= , CM000671.2:g.34648818A=	GRCh38
NC_000009.11:g.34648815A= , CM000671.1:g.34648815A=	GRCh37
NC_000009.10:g.34638815A=	NCBI36
NG_009029.1:g.7181A=
NG_028966.1:g.1634A=
NG_009029.2:g.7230A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*332A=	ENSP00000509954.1:n.*332A=
ENST00000378842.8:c.744A= MANE Select	ENSP00000368119.4:p.Thr248=
ENST00000378842.7:c.744A=	ENSP00000368119.3:p.Thr248=
ENST00000450095.6:c.417A=	ENSP00000401956.2:p.Thr139=
ENST00000473506.6:c.*332A=	ENSP00000432839.2:n.*332A=
ENST00000473529.5:n.903A=
ENST00000487381.5:n.1434A=
ENST00000489643.6:n.824A=
ENST00000554085.5:c.*488A=	ENSP00000450419.1:n.*488A=
ENST00000554550.5:c.*364A=	ENSP00000451435.1:n.*364A=
ENST00000554638.5:n.1216A=
ENST00000555020.5:n.1205A=
ENST00000555086.5:n.748A=
ENST00000555754.1:n.89A=
ENST00000556244.1:c.731A=
ENST00000556278.1:c.432+362A=	ENSP00000451792.1:n.432+362A=
ENST00000557706.5:n.1306A=
NM_000155.3:c.744A=	NP_000146.2:p.Thr248=
NM_001258332.1:c.417A=	NP_001245261.1:p.Thr139=
NM_000155.4:c.744A= MANE Select	NP_000146.2:p.Thr248=
NM_001258332.2:c.417A=	NP_001245261.1:p.Thr139=