Canonical Allele Identifier: CA373282289

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648429C>G (hg19) ; chr9:g.34648432C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648432C>G , CM000671.2:g.34648432C>G	GRCh38
NC_000009.11:g.34648429C>G , CM000671.1:g.34648429C>G	GRCh37
NC_000009.10:g.34638429C>G	NCBI36
NG_009029.1:g.6795C>G
NG_028966.1:g.1248C>G
NG_009029.2:g.6844C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*251C>G	ENSP00000509954.1:n.*251C>G
ENST00000378842.8:c.663C>G MANE Select	ENSP00000368119.4:p.Tyr221Ter
ENST00000378842.7:c.663C>G	ENSP00000368119.3:p.Tyr221Ter
ENST00000450095.6:c.336C>G	ENSP00000401956.2:p.Tyr112Ter
ENST00000472111.5:n.919C>G
ENST00000473506.6:c.*251C>G	ENSP00000432839.2:n.*251C>G
ENST00000473529.5:n.822C>G
ENST00000487381.5:n.1048C>G
ENST00000489643.6:n.438C>G
ENST00000554085.5:c.*407C>G	ENSP00000450419.1:n.*407C>G
ENST00000554550.5:c.*283C>G	ENSP00000451435.1:n.*283C>G
ENST00000554638.5:n.1135C>G
ENST00000555020.5:n.819C>G
ENST00000555086.5:n.667C>G
ENST00000555214.5:n.484C>G
ENST00000555754.1:n.8C>G
ENST00000556244.1:c.650C>G
ENST00000556278.1:c.408C>G	ENSP00000451792.1:p.Tyr136Ter
ENST00000556494.5:n.784C>G
ENST00000557706.5:n.1225C>G
NM_000155.3:c.663C>G	NP_000146.2:p.Tyr221Ter
NM_001258332.1:c.336C>G	NP_001245261.1:p.Tyr112Ter
NM_000155.4:c.663C>G MANE Select	NP_000146.2:p.Tyr221Ter
NM_001258332.2:c.336C>G	NP_001245261.1:p.Tyr112Ter