Canonical Allele Identifier: CA1845639191

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648498C= , CM000671.2:g.34648498C=	GRCh38
NC_000009.11:g.34648495C= , CM000671.1:g.34648495C=	GRCh37
NC_000009.10:g.34638495C=	NCBI36
NG_009029.1:g.6861C=
NG_028966.1:g.1314C=
NG_009029.2:g.6910C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*275+42C=	ENSP00000509954.1:n.*275+42C=
ENST00000378842.8:c.687+42C= MANE Select	ENSP00000368119.4:n.687+42C=
ENST00000378842.7:c.687+42C=	ENSP00000368119.3:n.687+42C=
ENST00000450095.6:c.360+42C=	ENSP00000401956.2:n.360+42C=
ENST00000473506.6:c.*275+42C=	ENSP00000432839.2:n.*275+42C=
ENST00000473529.5:n.846+42C=
ENST00000487381.5:n.1114C=
ENST00000489643.6:n.504C=
ENST00000554085.5:c.*431+42C=	ENSP00000450419.1:n.*431+42C=
ENST00000554550.5:c.*307+42C=	ENSP00000451435.1:n.*307+42C=
ENST00000554638.5:n.1159+42C=
ENST00000555020.5:n.885C=
ENST00000555086.5:n.691+42C=
ENST00000555214.5:n.550C=
ENST00000555754.1:n.32+42C=
ENST00000556244.1:c.674+42C=
ENST00000556278.1:c.432+42C=	ENSP00000451792.1:n.432+42C=
ENST00000556494.5:n.850C=
ENST00000557706.5:n.1249+42C=
NM_000155.3:c.687+42C=	NP_000146.2:n.687+42C=
NM_001258332.1:c.360+42C=	NP_001245261.1:n.360+42C=
NM_000155.4:c.687+42C= MANE Select	NP_000146.2:n.687+42C=
NM_001258332.2:c.360+42C=	NP_001245261.1:n.360+42C=