Canonical Allele Identifier: CA2521044736
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648707_34648708insCCTTC , CM000671.2:g.34648707_34648708insCCTTC GRCh38
NC_000009.11:g.34648704_34648705insCCTTC , CM000671.1:g.34648704_34648705insCCTTC GRCh37
NC_000009.10:g.34638704_34638705insCCTTC NCBI36
NG_009029.1:g.7070_7071insCCTTC
NG_028966.1:g.1523_1524insCCTTC
NG_009029.2:g.7119_7120insCCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.*276-55_*276-54insCCTTC ENSP00000509954.1:n.*276-55_*276-54insCCTTC
ENST00000378842.8:c.688-55_688-54insCCTTC MANE Select ENSP00000368119.4:n.688-55_688-54insCCTTC
ENST00000378842.7:c.688-55_688-54insCCTTC ENSP00000368119.3:n.688-55_688-54insCCTTC
ENST00000450095.6:c.361-55_361-54insCCTTC ENSP00000401956.2:n.361-55_361-54insCCTTC
ENST00000473506.6:c.*276-55_*276-54insCCTTC ENSP00000432839.2:n.*276-55_*276-54insCCTTC
ENST00000473529.5:n.847-55_847-54insCCTTC
ENST00000487381.5:n.1323_1324insCCTTC
ENST00000489643.6:n.713_714insCCTTC
ENST00000554085.5:c.*432-55_*432-54insCCTTC ENSP00000450419.1:n.*432-55_*432-54insCCTTC
ENST00000554550.5:c.*308-55_*308-54insCCTTC ENSP00000451435.1:n.*308-55_*308-54insCCTTC
ENST00000554638.5:n.1160-55_1160-54insCCTTC
ENST00000555020.5:n.1094_1095insCCTTC
ENST00000555086.5:n.692-55_692-54insCCTTC
ENST00000555754.1:n.33-55_33-54insCCTTC
ENST00000556244.1:c.675-55_675-54insCCTTC
ENST00000556278.1:c.432+251_432+252insCCTTC ENSP00000451792.1:n.432+251_432+252insCCTTC
ENST00000557706.5:n.1250-55_1250-54insCCTTC
NM_000155.3:c.688-55_688-54insCCTTC NP_000146.2:n.688-55_688-54insCCTTC
NM_001258332.1:c.361-55_361-54insCCTTC NP_001245261.1:n.361-55_361-54insCCTTC
NM_000155.4:c.688-55_688-54insCCTTC MANE Select NP_000146.2:n.688-55_688-54insCCTTC
NM_001258332.2:c.361-55_361-54insCCTTC NP_001245261.1:n.361-55_361-54insCCTTC