Canonical Allele Identifier: CA373284035

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648883A>T (hg19) ; chr9:g.34648886A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648886A>T , CM000671.2:g.34648886A>T	GRCh38
NC_000009.11:g.34648883A>T , CM000671.1:g.34648883A>T	GRCh37
NC_000009.10:g.34638883A>T	NCBI36
NG_009029.1:g.7249A>T
NG_028966.1:g.1702A>T
NG_009029.2:g.7298A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*400A>T	ENSP00000509954.1:n.*400A>T
ENST00000378842.8:c.812A>T MANE Select	ENSP00000368119.4:p.Glu271Val
ENST00000378842.7:c.812A>T	ENSP00000368119.3:p.Glu271Val
ENST00000450095.6:c.485A>T	ENSP00000401956.2:p.Glu162Val
ENST00000473506.6:c.*400A>T	ENSP00000432839.2:n.*400A>T
ENST00000489643.6:n.892A>T
ENST00000554085.5:c.*556A>T	ENSP00000450419.1:n.*556A>T
ENST00000554550.5:c.*432A>T	ENSP00000451435.1:n.*432A>T
ENST00000554638.5:n.1284A>T
ENST00000555020.5:n.1273A>T
ENST00000555086.5:n.816A>T
ENST00000555754.1:n.157A>T
ENST00000556244.1:c.799A>T
ENST00000556278.1:c.432+430A>T	ENSP00000451792.1:n.432+430A>T
ENST00000557706.5:n.1374A>T
NM_000155.3:c.812A>T	NP_000146.2:p.Glu271Val
NM_001258332.1:c.485A>T	NP_001245261.1:p.Glu162Val
NM_000155.4:c.812A>T MANE Select	NP_000146.2:p.Glu271Val
NM_001258332.2:c.485A>T	NP_001245261.1:p.Glu162Val