Canonical Allele Identifier: CA21989096

Gene: CYP4A11

Linked Data

• dbSNP Id: rs553438578
• gnomAD v2: 1-47398973-A-AGT
• gnomAD v3: 1-46933301-A-AGT
• gnomAD v4: 1-46933301-A-AGT
• MyVariant Identifiers: chr1:g.47398973_47398974insGT (hg19) ; chr1:g.46933301_46933302insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933303_46933304dup , CM000663.2:g.46933303_46933304dup	GRCh38
NC_000001.10:g.47398975_47398976dup , CM000663.1:g.47398975_47398976dup	GRCh37
NC_000001.9:g.47171562_47171563dup	NCBI36
NG_007932.1:g.13182_13183dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-256_1223-255dup MANE Select	ENSP00000311095.4:n.1223-256_1223-255dup
ENST00000310638.8:c.1223-256_1223-255dup	ENSP00000311095.4:n.1223-256_1223-255dup
ENST00000371904.8:c.1226-256_1226-255dup	ENSP00000360971.4:n.1226-256_1226-255dup
ENST00000371905.1:c.1223-256_1223-255dup	ENSP00000360972.1:n.1223-256_1223-255dup
ENST00000462347.5:c.929-256_929-255dup	ENSP00000477495.1:n.929-256_929-255dup
ENST00000465874.5:c.*21-256_*21-255dup	ENSP00000476368.1:n.*21-256_*21-255dup
ENST00000468629.5:c.1127-466_1127-465dup	ENSP00000476619.1:n.1127-466_1127-465dup
ENST00000474458.5:c.743-466_743-465dup	ENSP00000476988.1:n.743-466_743-465dup
ENST00000475477.5:c.*82-466_*82-465dup	ENSP00000476854.1:n.*82-466_*82-465dup
NM_000778.3:c.1223-256_1223-255dup	NP_000769.2:n.1223-256_1223-255dup
XM_005270539.1:c.929-256_929-255dup	XP_005270596.1:n.929-256_929-255dup
XM_011540826.1:c.1241-256_1241-255dup	XP_011539128.1:n.1241-256_1241-255dup
XM_011540827.1:c.947-256_947-255dup	XP_011539129.1:n.947-256_947-255dup
XM_011540828.1:c.929-256_929-255dup	XP_011539130.1:n.929-256_929-255dup
XR_246241.1:n.1127-256_1127-255dup
XR_246242.1:n.1111-256_1111-255dup
NM_001319155.1:c.1127-256_1127-255dup	NP_001306084.1:n.1127-256_1127-255dup
NM_001363587.1:c.929-256_929-255dup	NP_001350516.1:n.929-256_929-255dup
NR_134988.1:n.928-256_928-255dup
NR_134989.1:n.1119-256_1119-255dup
NR_134990.1:n.1178-466_1178-465dup
NR_134991.1:n.1100-256_1100-255dup
NR_134992.1:n.794-466_794-465dup
NR_134993.1:n.928-466_928-465dup
NR_134994.1:n.1135-256_1135-255dup
XM_017000465.1:c.911-256_911-255dup	XP_016855954.1:n.911-256_911-255dup
XR_001737005.1:n.1266-466_1266-465dup
NM_000778.4:c.1223-256_1223-255dup MANE Select	NP_000769.2:n.1223-256_1223-255dup
NM_001319155.2:c.1127-256_1127-255dup	NP_001306084.1:n.1127-256_1127-255dup
NM_001363587.2:c.929-256_929-255dup	NP_001350516.1:n.929-256_929-255dup
NR_134988.2:n.920-256_920-255dup
NR_134989.2:n.1111-256_1111-255dup
NR_134990.2:n.1170-466_1170-465dup
NR_134991.2:n.1092-256_1092-255dup
NR_134992.2:n.786-466_786-465dup
NR_134993.2:n.920-466_920-465dup
NR_134994.2:n.1127-256_1127-255dup