Canonical Allele Identifier: CA1845635686

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647209A= , CM000671.2:g.34647209A=	GRCh38
NC_000009.11:g.34647206A= , CM000671.1:g.34647206A=	GRCh37
NC_000009.10:g.34637206A=	NCBI36
NG_009029.1:g.5572A=
NG_028966.1:g.25A=
NG_009029.2:g.5621A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.203A=	ENSP00000509954.1:p.His68=
ENST00000378842.8:c.203A= MANE Select	ENSP00000368119.4:p.His68=
ENST00000378842.7:c.203A=	ENSP00000368119.3:p.His68=
ENST00000450095.6:c.1A=	ENSP00000401956.2:p.Met1=
ENST00000465543.6:n.542A=
ENST00000468099.2:n.243A=
ENST00000472111.5:n.244A=
ENST00000473506.6:c.203A=	ENSP00000432839.2:p.His68=
ENST00000473529.5:n.250A=
ENST00000485531.1:n.196A=
ENST00000487381.5:n.229A=
ENST00000489643.6:n.233A=
ENST00000554085.5:c.203A=	ENSP00000450419.1:p.His68=
ENST00000554139.5:n.256A=
ENST00000554330.5:n.200A=
ENST00000554550.5:c.203A=	ENSP00000451435.1:p.His68=
ENST00000554638.5:n.227A=
ENST00000554897.5:c.203A=	ENSP00000450942.1:p.His68=
ENST00000554944.5:n.233A=
ENST00000555020.5:n.233A=
ENST00000555086.5:n.207A=
ENST00000555214.5:n.212A=
ENST00000556157.1:n.310A=
ENST00000556244.1:c.87A=
ENST00000556278.1:c.203A=	ENSP00000451792.1:p.His68=
ENST00000556403.5:n.216A=
ENST00000556494.5:n.235A=
ENST00000557541.5:n.396A=
ENST00000557706.5:n.317A=
NM_000155.3:c.203A=	NP_000146.2:p.His68=
NM_001258332.1:c.1A=	NP_001245261.1:p.Met1=
NM_000155.4:c.203A= MANE Select	NP_000146.2:p.His68=
NM_001258332.2:c.1A=	NP_001245261.1:p.Met1=