Canonical Allele Identifier: CA1845639988

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648878C= , CM000671.2:g.34648878C=	GRCh38
NC_000009.11:g.34648875C= , CM000671.1:g.34648875C=	GRCh37
NC_000009.10:g.34638875C=	NCBI36
NG_009029.1:g.7241C=
NG_028966.1:g.1694C=
NG_009029.2:g.7290C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*392C=	ENSP00000509954.1:n.*392C=
ENST00000378842.8:c.804C= MANE Select	ENSP00000368119.4:p.Thr268=
ENST00000378842.7:c.804C=	ENSP00000368119.3:p.Thr268=
ENST00000450095.6:c.477C=	ENSP00000401956.2:p.Thr159=
ENST00000473506.6:c.*392C=	ENSP00000432839.2:n.*392C=
ENST00000489643.6:n.884C=
ENST00000554085.5:c.*548C=	ENSP00000450419.1:n.*548C=
ENST00000554550.5:c.*424C=	ENSP00000451435.1:n.*424C=
ENST00000554638.5:n.1276C=
ENST00000555020.5:n.1265C=
ENST00000555086.5:n.808C=
ENST00000555754.1:n.149C=
ENST00000556244.1:c.791C=
ENST00000556278.1:c.432+422C=	ENSP00000451792.1:n.432+422C=
ENST00000557706.5:n.1366C=
NM_000155.3:c.804C=	NP_000146.2:p.Thr268=
NM_001258332.1:c.477C=	NP_001245261.1:p.Thr159=
NM_000155.4:c.804C= MANE Select	NP_000146.2:p.Thr268=
NM_001258332.2:c.477C=	NP_001245261.1:p.Thr159=