Canonical Allele Identifier: CA373279099

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647499A>T (hg19) ; chr9:g.34647502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647502A>T , CM000671.2:g.34647502A>T	GRCh38
NC_000009.11:g.34647499A>T , CM000671.1:g.34647499A>T	GRCh37
NC_000009.10:g.34637499A>T	NCBI36
NG_009029.1:g.5865A>T
NG_028966.1:g.318A>T
NG_009029.2:g.5914A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.263A>T	ENSP00000509954.1:p.Gln88Leu
ENST00000378842.8:c.263A>T MANE Select	ENSP00000368119.4:p.Gln88Leu
ENST00000378842.7:c.263A>T	ENSP00000368119.3:p.Gln88Leu
ENST00000450095.6:c.50+244A>T	ENSP00000401956.2:n.50+244A>T
ENST00000465543.6:n.602A>T
ENST00000468099.2:n.536A>T
ENST00000472111.5:n.304A>T
ENST00000473506.6:c.253-39A>T	ENSP00000432839.2:n.253-39A>T
ENST00000473529.5:n.310A>T
ENST00000485531.1:n.489A>T
ENST00000487381.5:n.522A>T
ENST00000489643.6:n.282+244A>T
ENST00000554085.5:c.*7A>T	ENSP00000450419.1:n.*7A>T
ENST00000554139.5:n.316A>T
ENST00000554330.5:n.250-39A>T
ENST00000554550.5:c.252+244A>T	ENSP00000451435.1:n.252+244A>T
ENST00000554638.5:n.520A>T
ENST00000554897.5:c.252+244A>T	ENSP00000450942.1:n.252+244A>T
ENST00000554944.5:n.283-39A>T
ENST00000555020.5:n.293A>T
ENST00000555086.5:n.267A>T
ENST00000555214.5:n.261+244A>T
ENST00000556157.1:n.387A>T
ENST00000556244.1:c.250A>T
ENST00000556278.1:c.252+244A>T	ENSP00000451792.1:n.252+244A>T
ENST00000556403.5:n.276A>T
ENST00000556494.5:n.295A>T
ENST00000557541.5:n.446-39A>T
ENST00000557706.5:n.610A>T
NM_000155.3:c.263A>T	NP_000146.2:p.Gln88Leu
NM_001258332.1:c.50+244A>T	NP_001245261.1:n.50+244A>T
NM_000155.4:c.263A>T MANE Select	NP_000146.2:p.Gln88Leu
NM_001258332.2:c.50+244A>T	NP_001245261.1:n.50+244A>T