Canonical Allele Identifier: CA400881073
Gene: COG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193386T>G , CM000679.2:g.73193386T>G GRCh38
NC_000017.10:g.71189525T>G , CM000679.1:g.71189525T>G GRCh37
NC_000017.9:g.68701120T>G NCBI36
NG_008971.1:g.5353T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.315+2T>G MANE Select ENSP00000299886.4:n.315+2T>G
ENST00000299886.8:c.315+2T>G ENSP00000299886.4:n.315+2T>G
ENST00000438720.7:c.313+2T>G
ENST00000582587.2:c.292+2T>G
ENST00000618996.4:c.315+2T>G ENSP00000479450.1:n.315+2T>G
NM_018714.2:c.315+2T>G NP_061184.1:n.315+2T>G
NM_018714.3:c.315+2T>G MANE Select NP_061184.1:n.315+2T>G