Canonical Allele Identifier: CA1519888829

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205098_186205101delinsTGCA , CM000666.2:g.186205098_186205101delinsTGCA	GRCh38
NC_000004.11:g.187126252_187126255delinsTGCA , CM000666.1:g.187126252_187126255delinsTGCA	GRCh37
NC_000004.10:g.187363246_187363249delinsTGCA	NCBI36
NG_007965.1:g.18579_18582delinsTGCA
NG_012095.2:g.1120_1123delinsTGCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-102_988-99delinsTGCA MANE Select	ENSP00000368079.4:n.988-102_988-99delinsT...
ENST00000378802.4:c.988-102_988-99delinsTGCA	ENSP00000368079.4:n.988-102_988-99delinsT...
ENST00000502665.1:n.222+40_222+43delinsTGCA
ENST00000507209.5:n.5584_5587delinsTGCA
ENST00000513354.5:n.78-102_78-99delinsTGCA
NM_207352.3:c.988-102_988-99delinsTGCA	NP_997235.3:n.988-102_988-99delinsTGCA
XM_005262935.2:c.988-102_988-99delinsTGCA	XP_005262992.1:n.988-102_988-99delinsTGCA...
XM_006714184.2:c.592-102_592-99delinsTGCA	XP_006714247.1:n.592-102_592-99delinsTGCA...
XM_005262935.4:c.988-102_988-99delinsTGCA	XP_005262992.1:n.988-102_988-99delinsTGCA...
XM_017008037.1:c.592-102_592-99delinsTGCA	XP_016863526.1:n.592-102_592-99delinsTGCA...
NM_207352.4:c.988-102_988-99delinsTGCA MANE Select	NP_997235.3:n.988-102_988-99delinsTGCA