Canonical Allele Identifier: CA2213320451
Gene: COG7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23416933G= , CM000678.2:g.23416933G= GRCh38
NC_000016.9:g.23428254G= , CM000678.1:g.23428254G= GRCh37
NC_000016.8:g.23335755G= NCBI36
NG_021287.1:g.41259C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307149.10:c.1292+34C= MANE Select ENSP00000305442.5:n.1292+34C=
ENST00000307149.9:c.1292+34C= ENSP00000305442.5:n.1292+34C=
ENST00000567821.1:n.327+34C=
NM_153603.3:c.1292+34C= NP_705831.1:n.1292+34C=
XR_429680.1:n.1508+34C=
XM_017023870.1:c.1097+34C= XP_016879359.1:n.1097+34C=
XR_002957852.1:n.1513+34C=
XR_429680.2:n.1513+34C=
NM_153603.4:c.1292+34C= MANE Select NP_705831.1:n.1292+34C=