Canonical Allele Identifier: CA2565993246

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932964C>A , CM000663.2:g.46932964C>A	GRCh38
NC_000001.10:g.47398636C>A , CM000663.1:g.47398636C>A	GRCh37
NC_000001.9:g.47171223C>A	NCBI36
NG_007932.1:g.13521G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1287+19G>T MANE Select	ENSP00000311095.4:n.1287+19G>T
ENST00000310638.8:c.1287+19G>T	ENSP00000311095.4:n.1287+19G>T
ENST00000371904.8:c.1290+19G>T	ENSP00000360971.4:n.1290+19G>T
ENST00000371905.1:c.1287+19G>T	ENSP00000360972.1:n.1287+19G>T
ENST00000462347.5:c.993+19G>T	ENSP00000477495.1:n.993+19G>T
ENST00000465874.5:c.*85+19G>T	ENSP00000476368.1:n.*85+19G>T
ENST00000468629.5:c.1127-127G>T	ENSP00000476619.1:n.1127-127G>T
ENST00000474458.5:c.743-127G>T	ENSP00000476988.1:n.743-127G>T
ENST00000475477.5:c.*82-127G>T	ENSP00000476854.1:n.*82-127G>T
NM_000778.3:c.1287+19G>T	NP_000769.2:n.1287+19G>T
XM_005270539.1:c.993+19G>T	XP_005270596.1:n.993+19G>T
XM_011540826.1:c.1305+19G>T	XP_011539128.1:n.1305+19G>T
XM_011540827.1:c.1011+19G>T	XP_011539129.1:n.1011+19G>T
XM_011540828.1:c.993+19G>T	XP_011539130.1:n.993+19G>T
XR_246241.1:n.1191+19G>T
XR_246242.1:n.1175+19G>T
NM_001319155.1:c.1191+19G>T	NP_001306084.1:n.1191+19G>T
NM_001363587.1:c.993+19G>T	NP_001350516.1:n.993+19G>T
NR_134988.1:n.992+19G>T
NR_134989.1:n.1183+19G>T
NR_134990.1:n.1178-127G>T
NR_134991.1:n.1164+19G>T
NR_134992.1:n.794-127G>T
NR_134993.1:n.928-127G>T
NR_134994.1:n.1199+19G>T
XM_017000465.1:c.975+19G>T	XP_016855954.1:n.975+19G>T
XR_001737005.1:n.1266-127G>T
NM_000778.4:c.1287+19G>T MANE Select	NP_000769.2:n.1287+19G>T
NM_001319155.2:c.1191+19G>T	NP_001306084.1:n.1191+19G>T
NM_001363587.2:c.993+19G>T	NP_001350516.1:n.993+19G>T
NR_134988.2:n.984+19G>T
NR_134989.2:n.1175+19G>T
NR_134990.2:n.1170-127G>T
NR_134991.2:n.1156+19G>T
NR_134992.2:n.786-127G>T
NR_134993.2:n.920-127G>T
NR_134994.2:n.1191+19G>T