Canonical Allele Identifier: CA2839349896

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647989_34647990insCCAG , CM000671.2:g.34647989_34647990insCCAG	GRCh38
NC_000009.11:g.34647986_34647987insCCAG , CM000671.1:g.34647986_34647987insCCAG	GRCh37
NC_000009.10:g.34637986_34637987insCCAG	NCBI36
NG_009029.1:g.6352_6353insCCAG
NG_028966.1:g.805_806insCCAG
NG_009029.2:g.6401_6402insCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*95+28_*95+29insCCAG	ENSP00000509954.1:n.*95+28_*95+29insCCAG
ENST00000378842.8:c.507+28_507+29insCCAG MANE Select	ENSP00000368119.4:n.507+28_507+29insCCAG
ENST00000378842.7:c.507+28_507+29insCCAG	ENSP00000368119.3:n.507+28_507+29insCCAG
ENST00000450095.6:c.180+28_180+29insCCAG	ENSP00000401956.2:n.180+28_180+29insCCAG
ENST00000465543.6:n.846+28_846+29insCCAG
ENST00000472111.5:n.763+28_763+29insCCAG
ENST00000473506.6:c.*95+28_*95+29insCCAG	ENSP00000432839.2:n.*95+28_*95+29insCCAG
ENST00000473529.5:n.643+28_643+29insCCAG
ENST00000485531.1:n.976_977insCCAG
ENST00000487381.5:n.892+28_892+29insCCAG
ENST00000489643.6:n.283-126_283-125insCCAG
ENST00000554085.5:c.*251+28_*251+29insCCAG	ENSP00000450419.1:n.*251+28_*251+29insCCAG
ENST00000554139.5:n.686+28_686+29insCCAG
ENST00000554550.5:c.*127+28_*127+29insCCAG	ENSP00000451435.1:n.*127+28_*127+29insCCAG
ENST00000554638.5:n.979+28_979+29insCCAG
ENST00000554897.5:c.*127+28_*127+29insCCAG	ENSP00000450942.1:n.*127+28_*127+29insCCAG
ENST00000554944.5:n.731_732insCCAG
ENST00000555020.5:n.663+28_663+29insCCAG
ENST00000555086.5:n.511+28_511+29insCCAG
ENST00000555214.5:n.262-59_262-58insCCAG
ENST00000556244.1:c.494+28_494+29insCCAG
ENST00000556278.1:c.253-126_253-125insCCAG	ENSP00000451792.1:n.253-126_253-125insCCAG
ENST00000556494.5:n.628+28_628+29insCCAG
ENST00000557706.5:n.1069+28_1069+29insCCAG
NM_000155.3:c.507+28_507+29insCCAG	NP_000146.2:n.507+28_507+29insCCAG
NM_001258332.1:c.180+28_180+29insCCAG	NP_001245261.1:n.180+28_180+29insCCAG
NM_000155.4:c.507+28_507+29insCCAG MANE Select	NP_000146.2:n.507+28_507+29insCCAG
NM_001258332.2:c.180+28_180+29insCCAG	NP_001245261.1:n.180+28_180+29insCCAG