Canonical Allele Identifier: CA373283997

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648873A>T (hg19) ; chr9:g.34648876A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648876A>T , CM000671.2:g.34648876A>T	GRCh38
NC_000009.11:g.34648873A>T , CM000671.1:g.34648873A>T	GRCh37
NC_000009.10:g.34638873A>T	NCBI36
NG_009029.1:g.7239A>T
NG_028966.1:g.1692A>T
NG_009029.2:g.7288A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*390A>T	ENSP00000509954.1:n.*390A>T
ENST00000378842.8:c.802A>T MANE Select	ENSP00000368119.4:p.Thr268Ser
ENST00000378842.7:c.802A>T	ENSP00000368119.3:p.Thr268Ser
ENST00000450095.6:c.475A>T	ENSP00000401956.2:p.Thr159Ser
ENST00000473506.6:c.*390A>T	ENSP00000432839.2:n.*390A>T
ENST00000489643.6:n.882A>T
ENST00000554085.5:c.*546A>T	ENSP00000450419.1:n.*546A>T
ENST00000554550.5:c.*422A>T	ENSP00000451435.1:n.*422A>T
ENST00000554638.5:n.1274A>T
ENST00000555020.5:n.1263A>T
ENST00000555086.5:n.806A>T
ENST00000555754.1:n.147A>T
ENST00000556244.1:c.789A>T
ENST00000556278.1:c.432+420A>T	ENSP00000451792.1:n.432+420A>T
ENST00000557706.5:n.1364A>T
NM_000155.3:c.802A>T	NP_000146.2:p.Thr268Ser
NM_001258332.1:c.475A>T	NP_001245261.1:p.Thr159Ser
NM_000155.4:c.802A>T MANE Select	NP_000146.2:p.Thr268Ser
NM_001258332.2:c.475A>T	NP_001245261.1:p.Thr159Ser