Canonical Allele Identifier: CA340223155

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398463T>G (hg19) ; chr1:g.46932791T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932791T>G , CM000663.2:g.46932791T>G	GRCh38
NC_000001.10:g.47398463T>G , CM000663.1:g.47398463T>G	GRCh37
NC_000001.9:g.47171050T>G	NCBI36
NG_007932.1:g.13694A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1334A>C MANE Select	ENSP00000311095.4:p.His445Pro
ENST00000310638.8:c.1334A>C	ENSP00000311095.4:p.His445Pro
ENST00000371904.8:c.1337A>C	ENSP00000360971.4:p.His446Pro
ENST00000371905.1:c.1334A>C	ENSP00000360972.1:p.His445Pro
ENST00000462347.5:c.1040A>C	ENSP00000477495.1:p.His347Pro
ENST00000465874.5:c.*132A>C	ENSP00000476368.1:n.*132A>C
ENST00000468629.5:c.*39A>C	ENSP00000476619.1:n.*39A>C
ENST00000474458.5:c.*39A>C	ENSP00000476988.1:n.*39A>C
ENST00000475477.5:c.*128A>C	ENSP00000476854.1:n.*128A>C
NM_000778.3:c.1334A>C	NP_000769.2:p.His445Pro
XM_005270539.1:c.1040A>C	XP_005270596.1:p.His347Pro
XM_011540826.1:c.1352A>C	XP_011539128.1:p.His451Pro
XM_011540827.1:c.1058A>C	XP_011539129.1:p.His353Pro
XM_011540828.1:c.1040A>C	XP_011539130.1:p.His347Pro
XR_246241.1:n.1238A>C
XR_246242.1:n.1222A>C
NM_001319155.1:c.1238A>C	NP_001306084.1:p.His413Pro
NM_001363587.1:c.1040A>C	NP_001350516.1:p.His347Pro
NR_134988.1:n.1039A>C
NR_134989.1:n.1230A>C
NR_134990.1:n.1224A>C
NR_134991.1:n.1211A>C
NR_134992.1:n.840A>C
NR_134993.1:n.974A>C
NR_134994.1:n.1246A>C
XM_017000465.1:c.1022A>C	XP_016855954.1:p.His341Pro
XR_001737005.1:n.1312A>C
NM_000778.4:c.1334A>C MANE Select	NP_000769.2:p.His445Pro
NM_001319155.2:c.1238A>C	NP_001306084.1:p.His413Pro
NM_001363587.2:c.1040A>C	NP_001350516.1:p.His347Pro
NR_134988.2:n.1031A>C
NR_134989.2:n.1222A>C
NR_134990.2:n.1216A>C
NR_134991.2:n.1203A>C
NR_134992.2:n.832A>C
NR_134993.2:n.966A>C
NR_134994.2:n.1238A>C