Canonical Allele Identifier: CA1519888813

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205076_186205079delinsTTTC , CM000666.2:g.186205076_186205079delinsTTTC	GRCh38
NC_000004.11:g.187126230_187126233delinsTTTC , CM000666.1:g.187126230_187126233delinsTTTC	GRCh37
NC_000004.10:g.187363224_187363227delinsTTTC	NCBI36
NG_007965.1:g.18557_18560delinsTTTC
NG_012095.2:g.1098_1101delinsTTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-124_988-121delinsTTTC MANE Select	ENSP00000368079.4:n.988-124_988-121delins...
ENST00000378802.4:c.988-124_988-121delinsTTTC	ENSP00000368079.4:n.988-124_988-121delins...
ENST00000502665.1:n.222+18_222+21delinsTTTC
ENST00000507209.5:n.5562_5565delinsTTTC
ENST00000513354.5:n.78-124_78-121delinsTTTC
NM_207352.3:c.988-124_988-121delinsTTTC	NP_997235.3:n.988-124_988-121delinsTTTC
XM_005262935.2:c.988-124_988-121delinsTTTC	XP_005262992.1:n.988-124_988-121delinsTTT...
XM_006714184.2:c.592-124_592-121delinsTTTC	XP_006714247.1:n.592-124_592-121delinsTTT...
XM_005262935.4:c.988-124_988-121delinsTTTC	XP_005262992.1:n.988-124_988-121delinsTTT...
XM_017008037.1:c.592-124_592-121delinsTTTC	XP_016863526.1:n.592-124_592-121delinsTTT...
NM_207352.4:c.988-124_988-121delinsTTTC MANE Select	NP_997235.3:n.988-124_988-121delinsTTTC