Canonical Allele Identifier: CA1845641459

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649494_34649496delinsCCA , CM000671.2:g.34649494_34649496delinsCCA	GRCh38
NC_000009.11:g.34649491_34649493delinsCCA , CM000671.1:g.34649491_34649493delinsCCA	GRCh37
NC_000009.10:g.34639491_34639493delinsCCA	NCBI36
NG_009029.1:g.7857_7859delinsCCA
NG_028966.1:g.2310_2312delinsCCA
NG_009029.2:g.7906_7908delinsCCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*577_*579delinsCCA	ENSP00000509954.1:n.*577_*579delinsCCA
ENST00000378842.8:c.989_991delinsCCA MANE Select	ENSP00000368119.4:p.Ala330=
ENST00000378842.7:c.989_991delinsCCA	ENSP00000368119.3:p.Ala330=
ENST00000450095.6:c.662_664delinsCCA	ENSP00000401956.2:p.Ala221=
ENST00000488412.2:n.573_575delinsCCA
ENST00000489643.6:n.1397_1399delinsCCA
ENST00000554550.5:c.*609_*611delinsCCA	ENSP00000451435.1:n.*609_*611delinsCCA
ENST00000554638.5:n.1461_1463delinsCCA
ENST00000555020.5:n.1778_1780delinsCCA
ENST00000555754.1:n.437_439delinsCCA
ENST00000556278.1:c.432+1038_432+1040delinsCCA	ENSP00000451792.1:n.432+1038_432+1040deli...
ENST00000557706.5:n.1564_1566delinsCCA
NM_000155.3:c.989_991delinsCCA	NP_000146.2:p.Ala330=
NM_001258332.1:c.662_664delinsCCA	NP_001245261.1:p.Ala221=
NM_000155.4:c.989_991delinsCCA MANE Select	NP_000146.2:p.Ala330=
NM_001258332.2:c.662_664delinsCCA	NP_001245261.1:p.Ala221=