Canonical Allele Identifier: CA1845641285

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649473A= , CM000671.2:g.34649473A=	GRCh38
NC_000009.11:g.34649470A= , CM000671.1:g.34649470A=	GRCh37
NC_000009.10:g.34639470A=	NCBI36
NG_009029.1:g.7836A=
NG_028966.1:g.2289A=
NG_009029.2:g.7885A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*556A=	ENSP00000509954.1:n.*556A=
ENST00000378842.8:c.968A= MANE Select	ENSP00000368119.4:p.Tyr323=
ENST00000378842.7:c.968A=	ENSP00000368119.3:p.Tyr323=
ENST00000450095.6:c.641A=	ENSP00000401956.2:p.Tyr214=
ENST00000488412.2:n.552A=
ENST00000489643.6:n.1376A=
ENST00000554550.5:c.*588A=	ENSP00000451435.1:n.*588A=
ENST00000554638.5:n.1440A=
ENST00000555020.5:n.1757A=
ENST00000555754.1:n.416A=
ENST00000556278.1:c.432+1017A=	ENSP00000451792.1:n.432+1017A=
ENST00000557706.5:n.1543A=
NM_000155.3:c.968A=	NP_000146.2:p.Tyr323=
NM_001258332.1:c.641A=	NP_001245261.1:p.Tyr214=
NM_000155.4:c.968A= MANE Select	NP_000146.2:p.Tyr323=
NM_001258332.2:c.641A=	NP_001245261.1:p.Tyr214=