Canonical Allele Identifier: CA464402135

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648381T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648384T>G , CM000671.2:g.34648384T>G	GRCh38
NC_000009.11:g.34648381T>G , CM000671.1:g.34648381T>G	GRCh37
NC_000009.10:g.34638381T>G	NCBI36
NG_009029.1:g.6747T>G
NG_028966.1:g.1200T>G
NG_009029.2:g.6796T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*203T>G	ENSP00000509954.1:n.*203T>G
ENST00000378842.8:c.615T>G MANE Select	ENSP00000368119.4:p.Ser205=
ENST00000378842.7:c.615T>G	ENSP00000368119.3:p.Ser205=
ENST00000450095.6:c.288T>G	ENSP00000401956.2:p.Ser96=
ENST00000472111.5:n.871T>G
ENST00000473506.6:c.*203T>G	ENSP00000432839.2:n.*203T>G
ENST00000473529.5:n.774T>G
ENST00000487381.5:n.1000T>G
ENST00000489643.6:n.390T>G
ENST00000554085.5:c.*359T>G	ENSP00000450419.1:n.*359T>G
ENST00000554550.5:c.*235T>G	ENSP00000451435.1:n.*235T>G
ENST00000554638.5:n.1087T>G
ENST00000554944.5:n.964T>G
ENST00000555020.5:n.771T>G
ENST00000555086.5:n.619T>G
ENST00000555214.5:n.436T>G
ENST00000556244.1:c.602T>G
ENST00000556278.1:c.360T>G	ENSP00000451792.1:p.Ser120=
ENST00000556494.5:n.736T>G
ENST00000557706.5:n.1177T>G
NM_000155.3:c.615T>G	NP_000146.2:p.Ser205=
NM_001258332.1:c.288T>G	NP_001245261.1:p.Ser96=
NM_000155.4:c.615T>G MANE Select	NP_000146.2:p.Ser205=
NM_001258332.2:c.288T>G	NP_001245261.1:p.Ser96=