Canonical Allele Identifier: CA1845638981

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648432C= , CM000671.2:g.34648432C=	GRCh38
NC_000009.11:g.34648429C= , CM000671.1:g.34648429C=	GRCh37
NC_000009.10:g.34638429C=	NCBI36
NG_009029.1:g.6795C=
NG_028966.1:g.1248C=
NG_009029.2:g.6844C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*251C=	ENSP00000509954.1:n.*251C=
ENST00000378842.8:c.663C= MANE Select	ENSP00000368119.4:p.Tyr221=
ENST00000378842.7:c.663C=	ENSP00000368119.3:p.Tyr221=
ENST00000450095.6:c.336C=	ENSP00000401956.2:p.Tyr112=
ENST00000472111.5:n.919C=
ENST00000473506.6:c.*251C=	ENSP00000432839.2:n.*251C=
ENST00000473529.5:n.822C=
ENST00000487381.5:n.1048C=
ENST00000489643.6:n.438C=
ENST00000554085.5:c.*407C=	ENSP00000450419.1:n.*407C=
ENST00000554550.5:c.*283C=	ENSP00000451435.1:n.*283C=
ENST00000554638.5:n.1135C=
ENST00000555020.5:n.819C=
ENST00000555086.5:n.667C=
ENST00000555214.5:n.484C=
ENST00000555754.1:n.8C=
ENST00000556244.1:c.650C=
ENST00000556278.1:c.408C=	ENSP00000451792.1:p.Tyr136=
ENST00000556494.5:n.784C=
ENST00000557706.5:n.1225C=
NM_000155.3:c.663C=	NP_000146.2:p.Tyr221=
NM_001258332.1:c.336C=	NP_001245261.1:p.Tyr112=
NM_000155.4:c.663C= MANE Select	NP_000146.2:p.Tyr221=
NM_001258332.2:c.336C=	NP_001245261.1:p.Tyr112=