Canonical Allele Identifier: CA1845636577

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647694T= , CM000671.2:g.34647694T=	GRCh38
NC_000009.11:g.34647691T= , CM000671.1:g.34647691T=	GRCh37
NC_000009.10:g.34637691T=	NCBI36
NG_009029.1:g.6057T=
NG_028966.1:g.510T=
NG_009029.2:g.6106T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+127T=	ENSP00000509954.1:n.328+127T=
ENST00000378842.8:c.366T= MANE Select	ENSP00000368119.4:p.Ala122=
ENST00000378842.7:c.366T=	ENSP00000368119.3:p.Ala122=
ENST00000450095.6:c.51-138T=	ENSP00000401956.2:n.51-138T=
ENST00000465543.6:n.705T=
ENST00000472111.5:n.496T=
ENST00000473506.6:c.317T=	ENSP00000432839.2:p.Leu106=
ENST00000473529.5:n.502T=
ENST00000485531.1:n.681T=
ENST00000487381.5:n.625T=
ENST00000489643.6:n.283-421T=
ENST00000554085.5:c.*110T=	ENSP00000450419.1:n.*110T=
ENST00000554139.5:n.419T=
ENST00000554330.5:n.403T=
ENST00000554550.5:c.253-138T=	ENSP00000451435.1:n.253-138T=
ENST00000554638.5:n.712T=
ENST00000554897.5:c.253-138T=	ENSP00000450942.1:n.253-138T=
ENST00000554944.5:n.436T=
ENST00000555020.5:n.396T=
ENST00000555086.5:n.370T=
ENST00000555214.5:n.262-354T=
ENST00000556157.1:n.490T=
ENST00000556244.1:c.353T=
ENST00000556278.1:c.253-421T=	ENSP00000451792.1:n.253-421T=
ENST00000556403.5:n.468T=
ENST00000556494.5:n.487T=
ENST00000557541.5:n.510T=
ENST00000557706.5:n.802T=
NM_000155.3:c.366T=	NP_000146.2:p.Ala122=
NM_001258332.1:c.51-138T=	NP_001245261.1:n.51-138T=
NM_000155.4:c.366T= MANE Select	NP_000146.2:p.Ala122=
NM_001258332.2:c.51-138T=	NP_001245261.1:n.51-138T=