Canonical Allele Identifier: CA340223268

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1343185691
• gnomAD v2: 1-47398657-C-G
• gnomAD v3: 1-46932985-C-G
• gnomAD v4: 1-46932985-C-G
• MyVariant Identifiers: chr1:g.47398657C>G (hg19) ; chr1:g.46932985C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932985C>G , CM000663.2:g.46932985C>G	GRCh38
NC_000001.10:g.47398657C>G , CM000663.1:g.47398657C>G	GRCh37
NC_000001.9:g.47171244C>G	NCBI36
NG_007932.1:g.13500G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1285G>C MANE Select	ENSP00000311095.4:p.Glu429Gln
ENST00000310638.8:c.1285G>C	ENSP00000311095.4:p.Glu429Gln
ENST00000371904.8:c.1288G>C	ENSP00000360971.4:p.Glu430Gln
ENST00000371905.1:c.1285G>C	ENSP00000360972.1:p.Glu429Gln
ENST00000462347.5:c.991G>C	ENSP00000477495.1:p.Glu331Gln
ENST00000465874.5:c.*83G>C	ENSP00000476368.1:n.*83G>C
ENST00000468629.5:c.1127-148G>C	ENSP00000476619.1:n.1127-148G>C
ENST00000474458.5:c.743-148G>C	ENSP00000476988.1:n.743-148G>C
ENST00000475477.5:c.*82-148G>C	ENSP00000476854.1:n.*82-148G>C
NM_000778.3:c.1285G>C	NP_000769.2:p.Glu429Gln
XM_005270539.1:c.991G>C	XP_005270596.1:p.Glu331Gln
XM_011540826.1:c.1303G>C	XP_011539128.1:p.Glu435Gln
XM_011540827.1:c.1009G>C	XP_011539129.1:p.Glu337Gln
XM_011540828.1:c.991G>C	XP_011539130.1:p.Glu331Gln
XR_246241.1:n.1189G>C
XR_246242.1:n.1173G>C
NM_001319155.1:c.1189G>C	NP_001306084.1:p.Glu397Gln
NM_001363587.1:c.991G>C	NP_001350516.1:p.Glu331Gln
NR_134988.1:n.990G>C
NR_134989.1:n.1181G>C
NR_134990.1:n.1178-148G>C
NR_134991.1:n.1162G>C
NR_134992.1:n.794-148G>C
NR_134993.1:n.928-148G>C
NR_134994.1:n.1197G>C
XM_017000465.1:c.973G>C	XP_016855954.1:p.Glu325Gln
XR_001737005.1:n.1266-148G>C
NM_000778.4:c.1285G>C MANE Select	NP_000769.2:p.Glu429Gln
NM_001319155.2:c.1189G>C	NP_001306084.1:p.Glu397Gln
NM_001363587.2:c.991G>C	NP_001350516.1:p.Glu331Gln
NR_134988.2:n.982G>C
NR_134989.2:n.1173G>C
NR_134990.2:n.1170-148G>C
NR_134991.2:n.1154G>C
NR_134992.2:n.786-148G>C
NR_134993.2:n.920-148G>C
NR_134994.2:n.1189G>C