Canonical Allele Identifier: CA2672897768
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197702_186197703insCATTA , CM000666.2:g.186197702_186197703insCATTA GRCh38
NC_000004.11:g.187118856_187118857insCATTA , CM000666.1:g.187118856_187118857insCATTA GRCh37
NC_000004.10:g.187355850_187355851insCATTA NCBI36
NG_007965.1:g.11183_11184insCATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.674+100_674+101insCATTA MANE Select ENSP00000368079.4:n.674+100_674+101insCATTA
ENST00000378802.4:c.674+100_674+101insCATTA ENSP00000368079.4:n.674+100_674+101insCATTA
ENST00000507209.5:n.1515+100_1515+101insCATTA
NM_207352.3:c.674+100_674+101insCATTA NP_997235.3:n.674+100_674+101insCATTA
XM_005262935.2:c.674+100_674+101insCATTA XP_005262992.1:n.674+100_674+101insCATTA
XM_006714184.2:c.278+100_278+101insCATTA XP_006714247.1:n.278+100_278+101insCATTA
XM_005262935.4:c.674+100_674+101insCATTA XP_005262992.1:n.674+100_674+101insCATTA
XM_017008037.1:c.278+100_278+101insCATTA XP_016863526.1:n.278+100_278+101insCATTA
NM_207352.4:c.674+100_674+101insCATTA MANE Select NP_997235.3:n.674+100_674+101insCATTA