Canonical Allele Identifier: CA2672898087
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

gnomAD v4: 4-186210333-T-TGTTC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210334_186210337dup , CM000666.2:g.186210334_186210337dup GRCh38
NC_000004.11:g.187131488_187131491dup , CM000666.1:g.187131488_187131491dup GRCh37
NC_000004.10:g.187368482_187368485dup NCBI36
NG_007965.1:g.23815_23818dup
NG_012095.2:g.6356_6359dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1406-135_1406-132dup (CYP4V2) MANE Select ENSP00000368079.4:n.1406-135_1406-132dup
ENST00000378802.4:c.1406-135_1406-132dup (CYP4V2) ENSP00000368079.4:n.1406-135_1406-132dup
ENST00000502665.1:n.641-135_641-132dup (CYP4V2)
ENST00000507209.5:n.6104-135_6104-132dup (CYP4V2)
ENST00000511608.5:c.201+1062_201+1065dup (KLKB1)
ENST00000513354.5:n.496-135_496-132dup (CYP4V2)
NM_207352.3:c.1406-135_1406-132dup (CYP4V2) NP_997235.3:n.1406-135_1406-132dup
XM_005262935.2:c.1403-135_1403-132dup (CYP4V2) XP_005262992.1:n.1403-135_1403-132dup
XM_006714184.2:c.1010-135_1010-132dup (CYP4V2) XP_006714247.1:n.1010-135_1010-132dup
XM_005262935.4:c.1403-135_1403-132dup (CYP4V2) XP_005262992.1:n.1403-135_1403-132dup
XM_017008037.1:c.1010-135_1010-132dup (CYP4V2) XP_016863526.1:n.1010-135_1010-132dup
NM_207352.4:c.1406-135_1406-132dup (CYP4V2) MANE Select NP_997235.3:n.1406-135_1406-132dup
Search 100 bp 5'
Search 100 bp 3'