Canonical Allele Identifier: CA1519919175
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197436_186197447delinsAGCAGGATGTAC , CM000666.2:g.186197436_186197447delinsAGCAGGATGTAC GRCh38
NC_000004.11:g.187118590_187118601delinsAGCAGGATGTAC , CM000666.1:g.187118590_187118601delinsAGCAGGATGTAC GRCh37
NC_000004.10:g.187355584_187355595delinsAGCAGGATGTAC NCBI36
NG_007965.1:g.10917_10928delinsAGCAGGATGTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-97_605-86delinsAGCAGGATGTAC MANE Select ENSP00000368079.4:n.605-97_605-86delinsAG...
ENST00000378802.4:c.605-97_605-86delinsAGCAGGATGTAC ENSP00000368079.4:n.605-97_605-86delinsAG...
ENST00000507209.5:n.1349_1360delinsAGCAGGATGTAC
NM_207352.3:c.605-97_605-86delinsAGCAGGATGTAC NP_997235.3:n.605-97_605-86delinsAGCAGGAT...
XM_005262935.2:c.605-97_605-86delinsAGCAGGATGTAC XP_005262992.1:n.605-97_605-86delinsAGCAG...
XM_006714184.2:c.209-97_209-86delinsAGCAGGATGTAC XP_006714247.1:n.209-97_209-86delinsAGCAG...
XM_005262935.4:c.605-97_605-86delinsAGCAGGATGTAC XP_005262992.1:n.605-97_605-86delinsAGCAG...
XM_017008037.1:c.209-97_209-86delinsAGCAGGATGTAC XP_016863526.1:n.209-97_209-86delinsAGCAG...
NM_207352.4:c.605-97_605-86delinsAGCAGGATGTAC MANE Select NP_997235.3:n.605-97_605-86delinsAGCAGGAT...