Canonical Allele Identifier: CA1123157724
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821194267

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34649332_34649333insACATC , CM000671.2:g.34649332_34649333insACATC GRCh38
NC_000009.11:g.34649329_34649330insACATC , CM000671.1:g.34649329_34649330insACATC GRCh37
NC_000009.10:g.34639329_34639330insACATC NCBI36
NG_009029.1:g.7695_7696insACATC
NG_028966.1:g.2148_2149insACATC
NG_009029.2:g.7744_7745insACATC

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*493-78_*493-77insACATC ENSP00000509954.1:n.*493-78_*493-77insACATC
ENST00000378842.8:c.905-78_905-77insACATC MANE Select ENSP00000368119.4:n.905-78_905-77insACATC
ENST00000378842.7:c.905-78_905-77insACATC ENSP00000368119.3:n.905-78_905-77insACATC
ENST00000450095.6:c.578-78_578-77insACATC ENSP00000401956.2:n.578-78_578-77insACATC
ENST00000488412.2:n.411_412insACATC
ENST00000489643.6:n.1235_1236insACATC
ENST00000554550.5:c.*525-78_*525-77insACATC ENSP00000451435.1:n.*525-78_*525-77insACATC
ENST00000554638.5:n.1377-78_1377-77insACATC
ENST00000555020.5:n.1616_1617insACATC
ENST00000555754.1:n.353-78_353-77insACATC
ENST00000556278.1:c.432+876_432+877insACATC ENSP00000451792.1:n.432+876_432+877insACATC
ENST00000557706.5:n.1480-78_1480-77insACATC
NM_000155.3:c.905-78_905-77insACATC NP_000146.2:n.905-78_905-77insACATC
NM_001258332.1:c.578-78_578-77insACATC NP_001245261.1:n.578-78_578-77insACATC
NM_000155.4:c.905-78_905-77insACATC MANE Select NP_000146.2:n.905-78_905-77insACATC
NM_001258332.2:c.578-78_578-77insACATC NP_001245261.1:n.578-78_578-77insACATC