Canonical Allele Identifier: CA2764867636

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204633_186204634insACTC , CM000666.2:g.186204633_186204634insACTC	GRCh38
NC_000004.11:g.187125787_187125788insACTC , CM000666.1:g.187125787_187125788insACTC	GRCh37
NC_000004.10:g.187362781_187362782insACTC	NCBI36
NG_007965.1:g.18114_18115insACTC
NG_012095.2:g.655_656insACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-567_988-566insACTC MANE Select	ENSP00000368079.4:n.988-567_988-566insACTC
ENST00000378802.4:c.988-567_988-566insACTC	ENSP00000368079.4:n.988-567_988-566insACTC
ENST00000507209.5:n.5119_5120insACTC
ENST00000513354.5:n.77+176_77+177insACTC
NM_207352.3:c.988-567_988-566insACTC	NP_997235.3:n.988-567_988-566insACTC
XM_005262935.2:c.988-567_988-566insACTC	XP_005262992.1:n.988-567_988-566insACTC
XM_006714184.2:c.592-567_592-566insACTC	XP_006714247.1:n.592-567_592-566insACTC
XM_005262935.4:c.988-567_988-566insACTC	XP_005262992.1:n.988-567_988-566insACTC
XM_017008037.1:c.592-567_592-566insACTC	XP_016863526.1:n.592-567_592-566insACTC
NM_207352.4:c.988-567_988-566insACTC MANE Select	NP_997235.3:n.988-567_988-566insACTC