Canonical Allele Identifier: CA2645486269

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46932960-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932960T>G , CM000663.2:g.46932960T>G	GRCh38
NC_000001.10:g.47398632T>G , CM000663.1:g.47398632T>G	GRCh37
NC_000001.9:g.47171219T>G	NCBI36
NG_007932.1:g.13525A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1287+23A>C MANE Select	ENSP00000311095.4:n.1287+23A>C
ENST00000310638.8:c.1287+23A>C	ENSP00000311095.4:n.1287+23A>C
ENST00000371904.8:c.1290+23A>C	ENSP00000360971.4:n.1290+23A>C
ENST00000371905.1:c.1287+23A>C	ENSP00000360972.1:n.1287+23A>C
ENST00000462347.5:c.993+23A>C	ENSP00000477495.1:n.993+23A>C
ENST00000465874.5:c.*85+23A>C	ENSP00000476368.1:n.*85+23A>C
ENST00000468629.5:c.1127-123A>C	ENSP00000476619.1:n.1127-123A>C
ENST00000474458.5:c.743-123A>C	ENSP00000476988.1:n.743-123A>C
ENST00000475477.5:c.*82-123A>C	ENSP00000476854.1:n.*82-123A>C
NM_000778.3:c.1287+23A>C	NP_000769.2:n.1287+23A>C
XM_005270539.1:c.993+23A>C	XP_005270596.1:n.993+23A>C
XM_011540826.1:c.1305+23A>C	XP_011539128.1:n.1305+23A>C
XM_011540827.1:c.1011+23A>C	XP_011539129.1:n.1011+23A>C
XM_011540828.1:c.993+23A>C	XP_011539130.1:n.993+23A>C
XR_246241.1:n.1191+23A>C
XR_246242.1:n.1175+23A>C
NM_001319155.1:c.1191+23A>C	NP_001306084.1:n.1191+23A>C
NM_001363587.1:c.993+23A>C	NP_001350516.1:n.993+23A>C
NR_134988.1:n.992+23A>C
NR_134989.1:n.1183+23A>C
NR_134990.1:n.1178-123A>C
NR_134991.1:n.1164+23A>C
NR_134992.1:n.794-123A>C
NR_134993.1:n.928-123A>C
NR_134994.1:n.1199+23A>C
XM_017000465.1:c.975+23A>C	XP_016855954.1:n.975+23A>C
XR_001737005.1:n.1266-123A>C
NM_000778.4:c.1287+23A>C MANE Select	NP_000769.2:n.1287+23A>C
NM_001319155.2:c.1191+23A>C	NP_001306084.1:n.1191+23A>C
NM_001363587.2:c.993+23A>C	NP_001350516.1:n.993+23A>C
NR_134988.2:n.984+23A>C
NR_134989.2:n.1175+23A>C
NR_134990.2:n.1170-123A>C
NR_134991.2:n.1156+23A>C
NR_134992.2:n.786-123A>C
NR_134993.2:n.920-123A>C
NR_134994.2:n.1191+23A>C