Canonical Allele Identifier: CA2764867808

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204733_186204734insA , CM000666.2:g.186204733_186204734insA	GRCh38
NC_000004.11:g.187125887_187125888insA , CM000666.1:g.187125887_187125888insA	GRCh37
NC_000004.10:g.187362881_187362882insA	NCBI36
NG_007965.1:g.18214_18215insA
NG_012095.2:g.755_756insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-467_988-466insA MANE Select	ENSP00000368079.4:n.988-467_988-466insA
ENST00000378802.4:c.988-467_988-466insA	ENSP00000368079.4:n.988-467_988-466insA
ENST00000507209.5:n.5219_5220insA
ENST00000513354.5:n.77+276_77+277insA
NM_207352.3:c.988-467_988-466insA	NP_997235.3:n.988-467_988-466insA
XM_005262935.2:c.988-467_988-466insA	XP_005262992.1:n.988-467_988-466insA
XM_006714184.2:c.592-467_592-466insA	XP_006714247.1:n.592-467_592-466insA
XM_005262935.4:c.988-467_988-466insA	XP_005262992.1:n.988-467_988-466insA
XM_017008037.1:c.592-467_592-466insA	XP_016863526.1:n.592-467_592-466insA
NM_207352.4:c.988-467_988-466insA MANE Select	NP_997235.3:n.988-467_988-466insA