Canonical Allele Identifier: CA736354277

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1359764585
• gnomAD v3: 1-46931148-G-A
• gnomAD v4: 1-46931148-G-A
• MyVariant Identifiers: chr1:g.47396820G>A (hg19) ; chr1:g.46931148G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46931148G>A , CM000663.2:g.46931148G>A	GRCh38
NC_000001.10:g.47396820G>A , CM000663.1:g.47396820G>A	GRCh37
NC_000001.9:g.47169407G>A	NCBI36
NG_007932.1:g.15337C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1365-838C>T MANE Select	ENSP00000311095.4:n.1365-838C>T
ENST00000310638.8:c.1365-838C>T	ENSP00000311095.4:n.1365-838C>T
ENST00000371904.8:c.1368-838C>T	ENSP00000360971.4:n.1368-838C>T
ENST00000462347.5:c.1071-838C>T	ENSP00000477495.1:n.1071-838C>T
ENST00000468629.5:c.*70-838C>T	ENSP00000476619.1:n.*70-838C>T
ENST00000474458.5:c.*70-838C>T	ENSP00000476988.1:n.*70-838C>T
ENST00000475477.5:c.*159-838C>T	ENSP00000476854.1:n.*159-838C>T
NM_000778.3:c.1365-838C>T	NP_000769.2:n.1365-838C>T
XM_011540826.1:c.1383-838C>T	XP_011539128.1:n.1383-838C>T
XM_011540827.1:c.1089-838C>T	XP_011539129.1:n.1089-838C>T
XM_011540828.1:c.1071-838C>T	XP_011539130.1:n.1071-838C>T
XR_246241.1:n.1269-838C>T
XR_246242.1:n.1253-838C>T
NM_001319155.1:c.1269-838C>T	NP_001306084.1:n.1269-838C>T
NM_001363587.1:c.1071-838C>T	NP_001350516.1:n.1071-838C>T
NR_134988.1:n.1070-838C>T
NR_134989.1:n.1261-838C>T
NR_134990.1:n.1255-838C>T
NR_134991.1:n.1242-838C>T
NR_134992.1:n.871-838C>T
NR_134993.1:n.1005-838C>T
NR_134994.1:n.1277-838C>T
XM_017000465.1:c.1053-838C>T	XP_016855954.1:n.1053-838C>T
XR_001737005.1:n.1343-838C>T
NM_000778.4:c.1365-838C>T MANE Select	NP_000769.2:n.1365-838C>T
NM_001319155.2:c.1269-838C>T	NP_001306084.1:n.1269-838C>T
NM_001363587.2:c.1071-838C>T	NP_001350516.1:n.1071-838C>T
NR_134988.2:n.1062-838C>T
NR_134989.2:n.1253-838C>T
NR_134990.2:n.1247-838C>T
NR_134991.2:n.1234-838C>T
NR_134992.2:n.863-838C>T
NR_134993.2:n.997-838C>T
NR_134994.2:n.1269-838C>T