Canonical Allele Identifier: CA2542292815

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648171_34648172insCTTTTTACCGAATGAA , CM000671.2:g.34648171_34648172insCTTTTTACCGAATGAA	GRCh38
NC_000009.11:g.34648168_34648169insCTTTTTACCGAATGAA , CM000671.1:g.34648168_34648169insCTTTTTACCGAATGAA	GRCh37
NC_000009.10:g.34638168_34638169insCTTTTTACCGAATGAA	NCBI36
NG_009029.1:g.6534_6535insCTTTTTACCGAATGAA
NG_028966.1:g.987_988insCTTTTTACCGAATGAA
NG_009029.2:g.6583_6584insCTTTTTACCGAATGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*152_*152+1insCTTTTTACCGAATGAA	ENSP00000509954.1:n.*152_*152+1insCTTTTTACCGAATGAA
ENST00000378842.8:c.564_564+1insCTTTTTACCGAATGAA MANE Select	ENSP00000368119.4:n.564_564+1insCTTTTTACCGAATGAA
ENST00000378842.7:c.564_564+1insCTTTTTACCGAATGAA	ENSP00000368119.3:n.564_564+1insCTTTTTACCGAATGAA
ENST00000450095.6:c.237_237+1insCTTTTTACCGAATGAA	ENSP00000401956.2:n.237_237+1insCTTTTTACCGAATGAA
ENST00000472111.5:n.820_820+1insCTTTTTACCGAATGAA
ENST00000473506.6:c.*152_*152+1insCTTTTTACCGAATGAA	ENSP00000432839.2:n.*152_*152+1insCTTTTTACCGAATGAA
ENST00000473529.5:n.723_723+1insCTTTTTACCGAATGAA
ENST00000485531.1:n.1158_1158+1insCTTTTTACCGAATGAA
ENST00000487381.5:n.949_949+1insCTTTTTACCGAATGAA
ENST00000489643.6:n.339_339+1insCTTTTTACCGAATGAA
ENST00000554085.5:c.*308_*308+1insCTTTTTACCGAATGAA	ENSP00000450419.1:n.*308_*308+1insCTTTTTACCGAATGAA
ENST00000554139.5:n.810_810+1insCTTTTTACCGAATGAA
ENST00000554550.5:c.*184_*184+1insCTTTTTACCGAATGAA	ENSP00000451435.1:n.*184_*184+1insCTTTTTACCGAATGAA
ENST00000554638.5:n.1036_1036+1insCTTTTTACCGAATGAA
ENST00000554897.5:c.*251_*251+1insCTTTTTACCGAATGAA	ENSP00000450942.1:n.*251_*251+1insCTTTTTACCGAATGAA
ENST00000554944.5:n.913_913+1insCTTTTTACCGAATGAA
ENST00000555020.5:n.720_720+1insCTTTTTACCGAATGAA
ENST00000555086.5:n.568_568+1insCTTTTTACCGAATGAA
ENST00000555214.5:n.385_385+1insCTTTTTACCGAATGAA
ENST00000556244.1:c.551_551+1insCTTTTTACCGAATGAA
ENST00000556278.1:c.309_309+1insCTTTTTACCGAATGAA	ENSP00000451792.1:n.309_309+1insCTTTTTACCGAATGAA
ENST00000556494.5:n.685_685+1insCTTTTTACCGAATGAA
ENST00000557706.5:n.1126_1126+1insCTTTTTACCGAATGAA
NM_000155.3:c.564_564+1insCTTTTTACCGAATGAA	NP_000146.2:n.564_564+1insCTTTTTACCGAATGAA
NM_001258332.1:c.237_237+1insCTTTTTACCGAATGAA	NP_001245261.1:n.237_237+1insCTTTTTACCGAATGAA
NM_000155.4:c.564_564+1insCTTTTTACCGAATGAA MANE Select	NP_000146.2:n.564_564+1insCTTTTTACCGAATGAA
NM_001258332.2:c.237_237+1insCTTTTTACCGAATGAA	NP_001245261.1:n.237_237+1insCTTTTTACCGAATGAA