Canonical Allele Identifier: CA341808022
Gene: VTCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.117147667C>G , CM000663.2:g.117147667C>G GRCh38
NC_000001.10:g.117690289C>G , CM000663.1:g.117690289C>G GRCh37
NC_000001.9:g.117491812C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369458.8:c.840G>C MANE Select ENSP00000358470.3:p.Met280Ile
ENST00000328189.7:c.492G>C ENSP00000328168.3:p.Met164Ile
ENST00000359008.8:c.849G>C ENSP00000351899.4:p.Met283Ile
ENST00000369458.7:c.840G>C ENSP00000358470.3:p.Met280Ile
ENST00000539893.5:c.555G>C ENSP00000444724.1:p.Met185Ile
NM_001253849.1:c.555G>C NP_001240778.1:p.Met185Ile
NM_001253850.1:c.492G>C NP_001240779.1:p.Met164Ile
NM_024626.3:c.840G>C NP_078902.2:p.Met280Ile
NR_045603.1:n.1035G>C
NR_045604.1:n.739G>C
XM_011542143.1:c.891G>C XP_011540445.1:p.Met297Ile
XM_011542144.1:c.894G>C XP_011540446.1:p.Met298Ile
XM_011542145.1:c.855G>C XP_011540447.1:p.Met285Ile
XM_011542143.2:c.990G>C XP_011540445.2:p.Met330Ile
XM_017002335.2:c.855G>C XP_016857824.1:p.Met285Ile
NM_024626.4:c.840G>C MANE Select NP_078902.2:p.Met280Ile
NR_045603.2:n.1002G>C
NR_045604.2:n.706G>C
NM_001253849.2:c.555G>C NP_001240778.1:p.Met185Ile
NM_001253850.2:c.492G>C NP_001240779.1:p.Met164Ile