Canonical Allele Identifier: CA1519919501

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197638_186197642delinsTATTG , CM000666.2:g.186197638_186197642delinsTATTG	GRCh38
NC_000004.11:g.187118792_187118796delinsTATTG , CM000666.1:g.187118792_187118796delinsTATTG	GRCh37
NC_000004.10:g.187355786_187355790delinsTATTG	NCBI36
NG_007965.1:g.11119_11123delinsTATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+36_674+40delinsTATTG MANE Select	ENSP00000368079.4:n.674+36_674+40delinsTATTG
ENST00000378802.4:c.674+36_674+40delinsTATTG	ENSP00000368079.4:n.674+36_674+40delinsTATTG
ENST00000507209.5:n.1515+36_1515+40delinsTATTG
NM_207352.3:c.674+36_674+40delinsTATTG	NP_997235.3:n.674+36_674+40delinsTATTG
XM_005262935.2:c.674+36_674+40delinsTATTG	XP_005262992.1:n.674+36_674+40delinsTATTG
XM_006714184.2:c.278+36_278+40delinsTATTG	XP_006714247.1:n.278+36_278+40delinsTATTG
XM_005262935.4:c.674+36_674+40delinsTATTG	XP_005262992.1:n.674+36_674+40delinsTATTG
XM_017008037.1:c.278+36_278+40delinsTATTG	XP_016863526.1:n.278+36_278+40delinsTATTG
NM_207352.4:c.674+36_674+40delinsTATTG MANE Select	NP_997235.3:n.674+36_674+40delinsTATTG