Canonical Allele Identifier: CA395119624
Gene: COG7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23417017A>C , CM000678.2:g.23417017A>C GRCh38
NC_000016.9:g.23428338A>C , CM000678.1:g.23428338A>C GRCh37
NC_000016.8:g.23335839A>C NCBI36
NG_021287.1:g.41175T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307149.10:c.1242T>G MANE Select ENSP00000305442.5:p.Asn414Lys
ENST00000307149.9:c.1242T>G ENSP00000305442.5:p.Asn414Lys
ENST00000567821.1:n.277T>G
NM_153603.3:c.1242T>G NP_705831.1:p.Asn414Lys
XR_429680.1:n.1458T>G
XM_017023870.1:c.1047T>G XP_016879359.1:p.Asn349Lys
XR_002957852.1:n.1463T>G
XR_429680.2:n.1463T>G
NM_153603.4:c.1242T>G MANE Select NP_705831.1:p.Asn414Lys