Canonical Allele Identifier: CA340223229

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46932828-G-A
• MyVariant Identifiers: chr1:g.47398500G>A (hg19) ; chr1:g.46932828G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1297C>T MANE Select	ENSP00000311095.4:p.Pro433Ser
ENST00000310638.8:c.1297C>T	ENSP00000311095.4:p.Pro433Ser
ENST00000371904.8:c.1300C>T	ENSP00000360971.4:p.Pro434Ser
ENST00000371905.1:c.1297C>T	ENSP00000360972.1:p.Pro433Ser
ENST00000462347.5:c.1003C>T	ENSP00000477495.1:p.Pro335Ser
ENST00000465874.5:c.*95C>T	ENSP00000476368.1:n.*95C>T
ENST00000468629.5:c.*2C>T	ENSP00000476619.1:n.*2C>T
ENST00000474458.5:c.*2C>T	ENSP00000476988.1:n.*2C>T
ENST00000475477.5:c.*91C>T	ENSP00000476854.1:n.*91C>T
NM_000778.3:c.1297C>T	NP_000769.2:p.Pro433Ser
XM_005270539.1:c.1003C>T	XP_005270596.1:p.Pro335Ser
XM_011540826.1:c.1315C>T	XP_011539128.1:p.Pro439Ser
XM_011540827.1:c.1021C>T	XP_011539129.1:p.Pro341Ser
XM_011540828.1:c.1003C>T	XP_011539130.1:p.Pro335Ser
XR_246241.1:n.1201C>T
XR_246242.1:n.1185C>T
NM_001319155.1:c.1201C>T	NP_001306084.1:p.Pro401Ser
NM_001363587.1:c.1003C>T	NP_001350516.1:p.Pro335Ser
NR_134988.1:n.1002C>T
NR_134989.1:n.1193C>T
NR_134990.1:n.1187C>T
NR_134991.1:n.1174C>T
NR_134992.1:n.803C>T
NR_134993.1:n.937C>T
NR_134994.1:n.1209C>T
XM_017000465.1:c.985C>T	XP_016855954.1:p.Pro329Ser
XR_001737005.1:n.1275C>T
NM_000778.4:c.1297C>T MANE Select	NP_000769.2:p.Pro433Ser
NM_001319155.2:c.1201C>T	NP_001306084.1:p.Pro401Ser
NM_001363587.2:c.1003C>T	NP_001350516.1:p.Pro335Ser
NR_134988.2:n.994C>T
NR_134989.2:n.1185C>T
NR_134990.2:n.1179C>T
NR_134991.2:n.1166C>T
NR_134992.2:n.795C>T
NR_134993.2:n.929C>T
NR_134994.2:n.1201C>T