Canonical Allele Identifier: CA414210998
Gene: C1GALT1C1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119761010T>G (hg19) chrX:g.120627155T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120627155T>G , CM000685.2:g.120627155T>G GRCh38
NC_000023.10:g.119761010T>G , CM000685.1:g.119761010T>G GRCh37
NC_000023.9:g.119645038T>G NCBI36
NG_016219.1:g.7996A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304661.6:c.12A>C MANE Select ENSP00000304364.5:p.Glu4Asp
ENST00000304661.5:c.12A>C ENSP00000304364.5:p.Glu4Asp
ENST00000371313.2:c.12A>C ENSP00000360363.2:p.Glu4Asp
NM_001011551.2:c.12A>C NP_001011551.1:p.Glu4Asp
NM_152692.4:c.12A>C NP_689905.1:p.Glu4Asp
NM_001011551.3:c.12A>C MANE Select NP_001011551.1:p.Glu4Asp
NM_152692.5:c.12A>C NP_689905.1:p.Glu4Asp
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