Canonical Allele Identifier: CA340223178

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398472T>G (hg19) ; chr1:g.46932800T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932800T>G , CM000663.2:g.46932800T>G	GRCh38
NC_000001.10:g.47398472T>G , CM000663.1:g.47398472T>G	GRCh37
NC_000001.9:g.47171059T>G	NCBI36
NG_007932.1:g.13685A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1325A>C MANE Select	ENSP00000311095.4:p.Gln442Pro
ENST00000310638.8:c.1325A>C	ENSP00000311095.4:p.Gln442Pro
ENST00000371904.8:c.1328A>C	ENSP00000360971.4:p.Gln443Pro
ENST00000371905.1:c.1325A>C	ENSP00000360972.1:p.Gln442Pro
ENST00000462347.5:c.1031A>C	ENSP00000477495.1:p.Gln344Pro
ENST00000465874.5:c.*123A>C	ENSP00000476368.1:n.*123A>C
ENST00000468629.5:c.*30A>C	ENSP00000476619.1:n.*30A>C
ENST00000474458.5:c.*30A>C	ENSP00000476988.1:n.*30A>C
ENST00000475477.5:c.*119A>C	ENSP00000476854.1:n.*119A>C
NM_000778.3:c.1325A>C	NP_000769.2:p.Gln442Pro
XM_005270539.1:c.1031A>C	XP_005270596.1:p.Gln344Pro
XM_011540826.1:c.1343A>C	XP_011539128.1:p.Gln448Pro
XM_011540827.1:c.1049A>C	XP_011539129.1:p.Gln350Pro
XM_011540828.1:c.1031A>C	XP_011539130.1:p.Gln344Pro
XR_246241.1:n.1229A>C
XR_246242.1:n.1213A>C
NM_001319155.1:c.1229A>C	NP_001306084.1:p.Gln410Pro
NM_001363587.1:c.1031A>C	NP_001350516.1:p.Gln344Pro
NR_134988.1:n.1030A>C
NR_134989.1:n.1221A>C
NR_134990.1:n.1215A>C
NR_134991.1:n.1202A>C
NR_134992.1:n.831A>C
NR_134993.1:n.965A>C
NR_134994.1:n.1237A>C
XM_017000465.1:c.1013A>C	XP_016855954.1:p.Gln338Pro
XR_001737005.1:n.1303A>C
NM_000778.4:c.1325A>C MANE Select	NP_000769.2:p.Gln442Pro
NM_001319155.2:c.1229A>C	NP_001306084.1:p.Gln410Pro
NM_001363587.2:c.1031A>C	NP_001350516.1:p.Gln344Pro
NR_134988.2:n.1022A>C
NR_134989.2:n.1213A>C
NR_134990.2:n.1207A>C
NR_134991.2:n.1194A>C
NR_134992.2:n.823A>C
NR_134993.2:n.957A>C
NR_134994.2:n.1229A>C