Canonical Allele Identifier: CA1845639479
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648748_34648750delinsTTC , CM000671.2:g.34648748_34648750delinsTTC GRCh38
NC_000009.11:g.34648745_34648747delinsTTC , CM000671.1:g.34648745_34648747delinsTTC GRCh37
NC_000009.10:g.34638745_34638747delinsTTC NCBI36
NG_009029.1:g.7111_7113delinsTTC
NG_028966.1:g.1564_1566delinsTTC
NG_009029.2:g.7160_7162delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*276-14_*276-12delinsTTC ENSP00000509954.1:n.*276-14_*276-12delins...
ENST00000378842.8:c.688-14_688-12delinsTTC MANE Select ENSP00000368119.4:n.688-14_688-12delinsTT...
ENST00000378842.7:c.688-14_688-12delinsTTC ENSP00000368119.3:n.688-14_688-12delinsTT...
ENST00000450095.6:c.361-14_361-12delinsTTC ENSP00000401956.2:n.361-14_361-12delinsTT...
ENST00000473506.6:c.*276-14_*276-12delinsTTC ENSP00000432839.2:n.*276-14_*276-12delins...
ENST00000473529.5:n.847-14_847-12delinsTTC
ENST00000487381.5:n.1364_1366delinsTTC
ENST00000489643.6:n.754_756delinsTTC
ENST00000554085.5:c.*432-14_*432-12delinsTTC ENSP00000450419.1:n.*432-14_*432-12delins...
ENST00000554550.5:c.*308-14_*308-12delinsTTC ENSP00000451435.1:n.*308-14_*308-12delins...
ENST00000554638.5:n.1160-14_1160-12delinsTTC
ENST00000555020.5:n.1135_1137delinsTTC
ENST00000555086.5:n.692-14_692-12delinsTTC
ENST00000555754.1:n.33-14_33-12delinsTTC
ENST00000556244.1:c.675-14_675-12delinsTTC
ENST00000556278.1:c.432+292_432+294delinsTTC ENSP00000451792.1:n.432+292_432+294delins...
ENST00000557706.5:n.1250-14_1250-12delinsTTC
NM_000155.3:c.688-14_688-12delinsTTC NP_000146.2:n.688-14_688-12delinsTTC
NM_001258332.1:c.361-14_361-12delinsTTC NP_001245261.1:n.361-14_361-12delinsTTC
NM_000155.4:c.688-14_688-12delinsTTC MANE Select NP_000146.2:n.688-14_688-12delinsTTC
NM_001258332.2:c.361-14_361-12delinsTTC NP_001245261.1:n.361-14_361-12delinsTTC