Canonical Allele Identifier: CA1845639970

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648873C= , CM000671.2:g.34648873C=	GRCh38
NC_000009.11:g.34648870C= , CM000671.1:g.34648870C=	GRCh37
NC_000009.10:g.34638870C=	NCBI36
NG_009029.1:g.7236C=
NG_028966.1:g.1689C=
NG_009029.2:g.7285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*387C=	ENSP00000509954.1:n.*387C=
ENST00000378842.8:c.799C= MANE Select	ENSP00000368119.4:p.Leu267=
ENST00000378842.7:c.799C=	ENSP00000368119.3:p.Leu267=
ENST00000450095.6:c.472C=	ENSP00000401956.2:p.Leu158=
ENST00000473506.6:c.*387C=	ENSP00000432839.2:n.*387C=
ENST00000489643.6:n.879C=
ENST00000554085.5:c.*543C=	ENSP00000450419.1:n.*543C=
ENST00000554550.5:c.*419C=	ENSP00000451435.1:n.*419C=
ENST00000554638.5:n.1271C=
ENST00000555020.5:n.1260C=
ENST00000555086.5:n.803C=
ENST00000555754.1:n.144C=
ENST00000556244.1:c.786C=
ENST00000556278.1:c.432+417C=	ENSP00000451792.1:n.432+417C=
ENST00000557706.5:n.1361C=
NM_000155.3:c.799C=	NP_000146.2:p.Leu267=
NM_001258332.1:c.472C=	NP_001245261.1:p.Leu158=
NM_000155.4:c.799C= MANE Select	NP_000146.2:p.Leu267=
NM_001258332.2:c.472C=	NP_001245261.1:p.Leu158=