Canonical Allele Identifier: CA2841055805

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647986_34647987insCC , CM000671.2:g.34647986_34647987insCC	GRCh38
NC_000009.11:g.34647983_34647984insCC , CM000671.1:g.34647983_34647984insCC	GRCh37
NC_000009.10:g.34637983_34637984insCC	NCBI36
NG_009029.1:g.6349_6350insCC
NG_028966.1:g.802_803insCC
NG_009029.2:g.6398_6399insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*95+25_*95+26insCC	ENSP00000509954.1:n.*95+25_*95+26insCC
ENST00000378842.8:c.507+25_507+26insCC MANE Select	ENSP00000368119.4:n.507+25_507+26insCC
ENST00000378842.7:c.507+25_507+26insCC	ENSP00000368119.3:n.507+25_507+26insCC
ENST00000450095.6:c.180+25_180+26insCC	ENSP00000401956.2:n.180+25_180+26insCC
ENST00000465543.6:n.846+25_846+26insCC
ENST00000472111.5:n.763+25_763+26insCC
ENST00000473506.6:c.*95+25_*95+26insCC	ENSP00000432839.2:n.*95+25_*95+26insCC
ENST00000473529.5:n.643+25_643+26insCC
ENST00000485531.1:n.973_974insCC
ENST00000487381.5:n.892+25_892+26insCC
ENST00000489643.6:n.283-129_283-128insCC
ENST00000554085.5:c.*251+25_*251+26insCC	ENSP00000450419.1:n.*251+25_*251+26insCC
ENST00000554139.5:n.686+25_686+26insCC
ENST00000554550.5:c.*127+25_*127+26insCC	ENSP00000451435.1:n.*127+25_*127+26insCC
ENST00000554638.5:n.979+25_979+26insCC
ENST00000554897.5:c.*127+25_*127+26insCC	ENSP00000450942.1:n.*127+25_*127+26insCC
ENST00000554944.5:n.728_729insCC
ENST00000555020.5:n.663+25_663+26insCC
ENST00000555086.5:n.511+25_511+26insCC
ENST00000555214.5:n.262-62_262-61insCC
ENST00000556244.1:c.494+25_494+26insCC
ENST00000556278.1:c.253-129_253-128insCC	ENSP00000451792.1:n.253-129_253-128insCC
ENST00000556494.5:n.628+25_628+26insCC
ENST00000557706.5:n.1069+25_1069+26insCC
NM_000155.3:c.507+25_507+26insCC	NP_000146.2:n.507+25_507+26insCC
NM_001258332.1:c.180+25_180+26insCC	NP_001245261.1:n.180+25_180+26insCC
NM_000155.4:c.507+25_507+26insCC MANE Select	NP_000146.2:n.507+25_507+26insCC
NM_001258332.2:c.180+25_180+26insCC	NP_001245261.1:n.180+25_180+26insCC