Canonical Allele Identifier: CA1519888899
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205167_186205168delinsTG , CM000666.2:g.186205167_186205168delinsTG GRCh38
NC_000004.11:g.187126321_187126322delinsTG , CM000666.1:g.187126321_187126322delinsTG GRCh37
NC_000004.10:g.187363315_187363316delinsTG NCBI36
NG_007965.1:g.18648_18649delinsTG
NG_012095.2:g.1189_1190delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-33_988-32delinsTG MANE Select ENSP00000368079.4:n.988-33_988-32delinsTG...
ENST00000378802.4:c.988-33_988-32delinsTG ENSP00000368079.4:n.988-33_988-32delinsTG...
ENST00000502665.1:n.223-33_223-32delinsTG
ENST00000507209.5:n.5653_5654delinsTG
ENST00000513354.5:n.78-33_78-32delinsTG
NM_207352.3:c.988-33_988-32delinsTG NP_997235.3:n.988-33_988-32delinsTG
XM_005262935.2:c.988-33_988-32delinsTG XP_005262992.1:n.988-33_988-32delinsTG
XM_006714184.2:c.592-33_592-32delinsTG XP_006714247.1:n.592-33_592-32delinsTG
XM_005262935.4:c.988-33_988-32delinsTG XP_005262992.1:n.988-33_988-32delinsTG
XM_017008037.1:c.592-33_592-32delinsTG XP_016863526.1:n.592-33_592-32delinsTG
NM_207352.4:c.988-33_988-32delinsTG MANE Select NP_997235.3:n.988-33_988-32delinsTG