Canonical Allele Identifier: CA373284759

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649436A>T (hg19) ; chr9:g.34649439A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649439A>T , CM000671.2:g.34649439A>T	GRCh38
NC_000009.11:g.34649436A>T , CM000671.1:g.34649436A>T	GRCh37
NC_000009.10:g.34639436A>T	NCBI36
NG_009029.1:g.7802A>T
NG_028966.1:g.2255A>T
NG_009029.2:g.7851A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*522A>T	ENSP00000509954.1:n.*522A>T
ENST00000378842.8:c.934A>T MANE Select	ENSP00000368119.4:p.Asn312Tyr
ENST00000378842.7:c.934A>T	ENSP00000368119.3:p.Asn312Tyr
ENST00000450095.6:c.607A>T	ENSP00000401956.2:p.Asn203Tyr
ENST00000488412.2:n.518A>T
ENST00000489643.6:n.1342A>T
ENST00000554550.5:c.*554A>T	ENSP00000451435.1:n.*554A>T
ENST00000554638.5:n.1406A>T
ENST00000555020.5:n.1723A>T
ENST00000555754.1:n.382A>T
ENST00000556278.1:c.432+983A>T	ENSP00000451792.1:n.432+983A>T
ENST00000557706.5:n.1509A>T
NM_000155.3:c.934A>T	NP_000146.2:p.Asn312Tyr
NM_001258332.1:c.607A>T	NP_001245261.1:p.Asn203Tyr
NM_000155.4:c.934A>T MANE Select	NP_000146.2:p.Asn312Tyr
NM_001258332.2:c.607A>T	NP_001245261.1:p.Asn203Tyr