Canonical Allele Identifier: CA373278911

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647248A>G (hg19) ; chr9:g.34647251A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647251A>G , CM000671.2:g.34647251A>G	GRCh38
NC_000009.11:g.34647248A>G , CM000671.1:g.34647248A>G	GRCh37
NC_000009.10:g.34637248A>G	NCBI36
NG_009029.1:g.5614A>G
NG_028966.1:g.67A>G
NG_009029.2:g.5663A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.245A>G	ENSP00000509954.1:p.Asn82Ser
ENST00000378842.8:c.245A>G MANE Select	ENSP00000368119.4:p.Asn82Ser
ENST00000378842.7:c.245A>G	ENSP00000368119.3:p.Asn82Ser
ENST00000450095.6:c.43A>G	ENSP00000401956.2:p.Thr15Ala
ENST00000465543.6:n.584A>G
ENST00000468099.2:n.285A>G
ENST00000472111.5:n.286A>G
ENST00000473506.6:c.245A>G	ENSP00000432839.2:p.Asn82Ser
ENST00000473529.5:n.292A>G
ENST00000485531.1:n.238A>G
ENST00000487381.5:n.271A>G
ENST00000489643.6:n.275A>G
ENST00000554085.5:c.245A>G	ENSP00000450419.1:p.Asn82Ser
ENST00000554139.5:n.298A>G
ENST00000554330.5:n.242A>G
ENST00000554550.5:c.245A>G	ENSP00000451435.1:p.Asn82Ser
ENST00000554638.5:n.269A>G
ENST00000554897.5:c.245A>G	ENSP00000450942.1:p.Asn82Ser
ENST00000554944.5:n.275A>G
ENST00000555020.5:n.275A>G
ENST00000555086.5:n.249A>G
ENST00000555214.5:n.254A>G
ENST00000556157.1:n.352A>G
ENST00000556244.1:c.129A>G
ENST00000556278.1:c.245A>G	ENSP00000451792.1:p.Asn82Ser
ENST00000556403.5:n.258A>G
ENST00000556494.5:n.277A>G
ENST00000557541.5:n.438A>G
ENST00000557706.5:n.359A>G
NM_000155.3:c.245A>G	NP_000146.2:p.Asn82Ser
NM_001258332.1:c.43A>G	NP_001245261.1:p.Thr15Ala
NM_000155.4:c.245A>G MANE Select	NP_000146.2:p.Asn82Ser
NM_001258332.2:c.43A>G	NP_001245261.1:p.Thr15Ala