Canonical Allele Identifier: CA2764867628

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204627_186204628insGTG , CM000666.2:g.186204627_186204628insGTG	GRCh38
NC_000004.11:g.187125781_187125782insGTG , CM000666.1:g.187125781_187125782insGTG	GRCh37
NC_000004.10:g.187362775_187362776insGTG	NCBI36
NG_007965.1:g.18108_18109insGTG
NG_012095.2:g.649_650insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-573_988-572insGTG MANE Select	ENSP00000368079.4:n.988-573_988-572insGTG
ENST00000378802.4:c.988-573_988-572insGTG	ENSP00000368079.4:n.988-573_988-572insGTG
ENST00000507209.5:n.5113_5114insGTG
ENST00000513354.5:n.77+170_77+171insGTG
NM_207352.3:c.988-573_988-572insGTG	NP_997235.3:n.988-573_988-572insGTG
XM_005262935.2:c.988-573_988-572insGTG	XP_005262992.1:n.988-573_988-572insGTG
XM_006714184.2:c.592-573_592-572insGTG	XP_006714247.1:n.592-573_592-572insGTG
XM_005262935.4:c.988-573_988-572insGTG	XP_005262992.1:n.988-573_988-572insGTG
XM_017008037.1:c.592-573_592-572insGTG	XP_016863526.1:n.592-573_592-572insGTG
NM_207352.4:c.988-573_988-572insGTG MANE Select	NP_997235.3:n.988-573_988-572insGTG