Canonical Allele Identifier: CA1845638621

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648357A= , CM000671.2:g.34648357A=	GRCh38
NC_000009.11:g.34648354A= , CM000671.1:g.34648354A=	GRCh37
NC_000009.10:g.34638354A=	NCBI36
NG_009029.1:g.6720A=
NG_028966.1:g.1173A=
NG_009029.2:g.6769A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*176A=	ENSP00000509954.1:n.*176A=
ENST00000378842.8:c.588A= MANE Select	ENSP00000368119.4:p.Pro196=
ENST00000378842.7:c.588A=	ENSP00000368119.3:p.Pro196=
ENST00000450095.6:c.261A=	ENSP00000401956.2:p.Pro87=
ENST00000472111.5:n.844A=
ENST00000473506.6:c.*176A=	ENSP00000432839.2:n.*176A=
ENST00000473529.5:n.747A=
ENST00000485531.1:n.1182A=
ENST00000487381.5:n.973A=
ENST00000489643.6:n.363A=
ENST00000554085.5:c.*332A=	ENSP00000450419.1:n.*332A=
ENST00000554139.5:n.834A=
ENST00000554550.5:c.*208A=	ENSP00000451435.1:n.*208A=
ENST00000554638.5:n.1060A=
ENST00000554897.5:c.*275A=	ENSP00000450942.1:n.*275A=
ENST00000554944.5:n.937A=
ENST00000555020.5:n.744A=
ENST00000555086.5:n.592A=
ENST00000555214.5:n.409A=
ENST00000556244.1:c.575A=
ENST00000556278.1:c.333A=	ENSP00000451792.1:p.Pro111=
ENST00000556494.5:n.709A=
ENST00000557706.5:n.1150A=
NM_000155.3:c.588A=	NP_000146.2:p.Pro196=
NM_001258332.1:c.261A=	NP_001245261.1:p.Pro87=
NM_000155.4:c.588A= MANE Select	NP_000146.2:p.Pro196=
NM_001258332.2:c.261A=	NP_001245261.1:p.Pro87=