Canonical Allele Identifier: CA1845638378

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648267_34648281delinsTGCCAATGATGTGGA , CM000671.2:g.34648267_34648281delinsTGCCAATGATGTGGA	GRCh38
NC_000009.11:g.34648264_34648278delinsTGCCAATGATGTGGA , CM000671.1:g.34648264_34648278delinsTGCCAATGATGTGGA	GRCh37
NC_000009.10:g.34638264_34638278delinsTGCCAATGATGTGGA	NCBI36
NG_009029.1:g.6630_6644delinsTGCCAATGATGTGGA
NG_028966.1:g.1083_1097delinsTGCCAATGATGTGGA
NG_009029.2:g.6679_6693delinsTGCCAATGATGTGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*153-67_*153-53delinsTGCCAATGATGTGGA	ENSP00000509954.1:n.*153-67_*153-53delins...
ENST00000378842.8:c.565-67_565-53delinsTGCCAATGATGTGGA MANE Select	ENSP00000368119.4:n.565-67_565-53delinsTG...
ENST00000378842.7:c.565-67_565-53delinsTGCCAATGATGTGGA	ENSP00000368119.3:n.565-67_565-53delinsTG...
ENST00000450095.6:c.238-67_238-53delinsTGCCAATGATGTGGA	ENSP00000401956.2:n.238-67_238-53delinsTG...
ENST00000472111.5:n.821-67_821-53delinsTGCCAATGATGTGGA
ENST00000473506.6:c.*153-67_*153-53delinsTGCCAATGATGTGGA	ENSP00000432839.2:n.*153-67_*153-53delins...
ENST00000473529.5:n.724-67_724-53delinsTGCCAATGATGTGGA
ENST00000485531.1:n.1159-67_1159-53delinsTGCCAATGATGTGGA
ENST00000487381.5:n.950-67_950-53delinsTGCCAATGATGTGGA
ENST00000489643.6:n.340-67_340-53delinsTGCCAATGATGTGGA
ENST00000554085.5:c.*309-67_*309-53delinsTGCCAATGATGTGGA	ENSP00000450419.1:n.*309-67_*309-53delins...
ENST00000554139.5:n.811-67_811-53delinsTGCCAATGATGTGGA
ENST00000554550.5:c.*185-67_*185-53delinsTGCCAATGATGTGGA	ENSP00000451435.1:n.*185-67_*185-53delins...
ENST00000554638.5:n.1037-67_1037-53delinsTGCCAATGATGTGGA
ENST00000554897.5:c.*252-67_*252-53delinsTGCCAATGATGTGGA	ENSP00000450942.1:n.*252-67_*252-53delins...
ENST00000554944.5:n.914-67_914-53delinsTGCCAATGATGTGGA
ENST00000555020.5:n.721-67_721-53delinsTGCCAATGATGTGGA
ENST00000555086.5:n.569-67_569-53delinsTGCCAATGATGTGGA
ENST00000555214.5:n.386-67_386-53delinsTGCCAATGATGTGGA
ENST00000556244.1:c.552-67_552-53delinsTGCCAATGATGTGGA
ENST00000556278.1:c.310-67_310-53delinsTGCCAATGATGTGGA	ENSP00000451792.1:n.310-67_310-53delinsTG...
ENST00000556494.5:n.686-67_686-53delinsTGCCAATGATGTGGA
ENST00000557706.5:n.1127-67_1127-53delinsTGCCAATGATGTGGA
NM_000155.3:c.565-67_565-53delinsTGCCAATGATGTGGA	NP_000146.2:n.565-67_565-53delinsTGCCAATG...
NM_001258332.1:c.238-67_238-53delinsTGCCAATGATGTGGA	NP_001245261.1:n.238-67_238-53delinsTGCCA...
NM_000155.4:c.565-67_565-53delinsTGCCAATGATGTGGA MANE Select	NP_000146.2:n.565-67_565-53delinsTGCCAATG...
NM_001258332.2:c.238-67_238-53delinsTGCCAATGATGTGGA	NP_001245261.1:n.238-67_238-53delinsTGCCA...