Canonical Allele Identifier: CA340223231

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398500G>T (hg19) ; chr1:g.46932828G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932828G>T , CM000663.2:g.46932828G>T	GRCh38
NC_000001.10:g.47398500G>T , CM000663.1:g.47398500G>T	GRCh37
NC_000001.9:g.47171087G>T	NCBI36
NG_007932.1:g.13657C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1297C>A MANE Select	ENSP00000311095.4:p.Pro433Thr
ENST00000310638.8:c.1297C>A	ENSP00000311095.4:p.Pro433Thr
ENST00000371904.8:c.1300C>A	ENSP00000360971.4:p.Pro434Thr
ENST00000371905.1:c.1297C>A	ENSP00000360972.1:p.Pro433Thr
ENST00000462347.5:c.1003C>A	ENSP00000477495.1:p.Pro335Thr
ENST00000465874.5:c.*95C>A	ENSP00000476368.1:n.*95C>A
ENST00000468629.5:c.*2C>A	ENSP00000476619.1:n.*2C>A
ENST00000474458.5:c.*2C>A	ENSP00000476988.1:n.*2C>A
ENST00000475477.5:c.*91C>A	ENSP00000476854.1:n.*91C>A
NM_000778.3:c.1297C>A	NP_000769.2:p.Pro433Thr
XM_005270539.1:c.1003C>A	XP_005270596.1:p.Pro335Thr
XM_011540826.1:c.1315C>A	XP_011539128.1:p.Pro439Thr
XM_011540827.1:c.1021C>A	XP_011539129.1:p.Pro341Thr
XM_011540828.1:c.1003C>A	XP_011539130.1:p.Pro335Thr
XR_246241.1:n.1201C>A
XR_246242.1:n.1185C>A
NM_001319155.1:c.1201C>A	NP_001306084.1:p.Pro401Thr
NM_001363587.1:c.1003C>A	NP_001350516.1:p.Pro335Thr
NR_134988.1:n.1002C>A
NR_134989.1:n.1193C>A
NR_134990.1:n.1187C>A
NR_134991.1:n.1174C>A
NR_134992.1:n.803C>A
NR_134993.1:n.937C>A
NR_134994.1:n.1209C>A
XM_017000465.1:c.985C>A	XP_016855954.1:p.Pro329Thr
XR_001737005.1:n.1275C>A
NM_000778.4:c.1297C>A MANE Select	NP_000769.2:p.Pro433Thr
NM_001319155.2:c.1201C>A	NP_001306084.1:p.Pro401Thr
NM_001363587.2:c.1003C>A	NP_001350516.1:p.Pro335Thr
NR_134988.2:n.994C>A
NR_134989.2:n.1185C>A
NR_134990.2:n.1179C>A
NR_134991.2:n.1166C>A
NR_134992.2:n.795C>A
NR_134993.2:n.929C>A
NR_134994.2:n.1201C>A