Canonical Allele Identifier: CA2213320455
Gene: COG7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23416937C= , CM000678.2:g.23416937C= GRCh38
NC_000016.9:g.23428258C= , CM000678.1:g.23428258C= GRCh37
NC_000016.8:g.23335759C= NCBI36
NG_021287.1:g.41255G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307149.10:c.1292+30G= MANE Select ENSP00000305442.5:n.1292+30G=
ENST00000307149.9:c.1292+30G= ENSP00000305442.5:n.1292+30G=
ENST00000567821.1:n.327+30G=
NM_153603.3:c.1292+30G= NP_705831.1:n.1292+30G=
XR_429680.1:n.1508+30G=
XM_017023870.1:c.1097+30G= XP_016879359.1:n.1097+30G=
XR_002957852.1:n.1513+30G=
XR_429680.2:n.1513+30G=
NM_153603.4:c.1292+30G= MANE Select NP_705831.1:n.1292+30G=
Search 100 bp 5'
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