Canonical Allele Identifier: CA2579371197

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647591G>T , CM000671.2:g.34647591G>T	GRCh38
NC_000009.11:g.34647588G>T , CM000671.1:g.34647588G>T	GRCh37
NC_000009.10:g.34637588G>T	NCBI36
NG_009029.1:g.5954G>T
NG_028966.1:g.407G>T
NG_009029.2:g.6003G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+24G>T	ENSP00000509954.1:n.328+24G>T
ENST00000378842.8:c.328+24G>T MANE Select	ENSP00000368119.4:n.328+24G>T
ENST00000378842.7:c.328+24G>T	ENSP00000368119.3:n.328+24G>T
ENST00000450095.6:c.51-241G>T	ENSP00000401956.2:n.51-241G>T
ENST00000465543.6:n.667+24G>T
ENST00000472111.5:n.393G>T
ENST00000473506.6:c.279+24G>T	ENSP00000432839.2:n.279+24G>T
ENST00000473529.5:n.399G>T
ENST00000485531.1:n.578G>T
ENST00000487381.5:n.587+24G>T
ENST00000489643.6:n.282+333G>T
ENST00000554085.5:c.*72+24G>T	ENSP00000450419.1:n.*72+24G>T
ENST00000554139.5:n.381+24G>T
ENST00000554330.5:n.300G>T
ENST00000554550.5:c.253-241G>T	ENSP00000451435.1:n.253-241G>T
ENST00000554638.5:n.609G>T
ENST00000554897.5:c.253-241G>T	ENSP00000450942.1:n.253-241G>T
ENST00000554944.5:n.333G>T
ENST00000555020.5:n.358+24G>T
ENST00000555086.5:n.332+24G>T
ENST00000555214.5:n.261+333G>T
ENST00000556157.1:n.452+24G>T
ENST00000556244.1:c.315+24G>T
ENST00000556278.1:c.252+333G>T	ENSP00000451792.1:n.252+333G>T
ENST00000556403.5:n.365G>T
ENST00000556494.5:n.384G>T
ENST00000557541.5:n.472+24G>T
ENST00000557706.5:n.699G>T
NM_000155.3:c.328+24G>T	NP_000146.2:n.328+24G>T
NM_001258332.1:c.51-241G>T	NP_001245261.1:n.51-241G>T
NM_000155.4:c.328+24G>T MANE Select	NP_000146.2:n.328+24G>T
NM_001258332.2:c.51-241G>T	NP_001245261.1:n.51-241G>T