Canonical Allele Identifier: CA213397
Gene: HSD11B1 HGNC NCBI
HSD11B1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209706873dup , CM000663.2:g.209706873dup GRCh38
NC_000001.10:g.209880218dup , CM000663.1:g.209880218dup GRCh37
NC_000001.9:g.207946841dup NCBI36
NG_012081.1:g.25669dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367027.5:c.331+53dup (HSD11B1) MANE Select ENSP00000355994.3:n.331+53dup
ENST00000261465.5:c.331+53dup (HSD11B1) ENSP00000261465.2:n.331+53dup
ENST00000367027.4:c.331+53dup (HSD11B1) ENSP00000355994.3:n.331+53dup
ENST00000367028.6:c.331+53dup (HSD11B1) ENSP00000355995.1:n.331+53dup
ENST00000615289.4:c.331+53dup (HSD11B1) ENSP00000478430.1:n.331+53dup
NM_001206741.1:c.331+53dup (HSD11B1) NP_001193670.1:n.331+53dup
NM_005525.3:c.331+53dup (HSD11B1) NP_005516.1:n.331+53dup
NM_181755.2:c.331+53dup (HSD11B1) NP_861420.1:n.331+53dup
XR_922542.1:n.3234+17158dup (HSD11B1-AS1)
XR_922543.1:n.3225+17158dup (HSD11B1-AS1)
XR_922547.1:n.3090+35625dup (HSD11B1-AS1)
XR_922549.1:n.125-43811dup (HSD11B1-AS1)
NR_134509.1:n.96+17158dup (HSD11B1-AS1)
NR_134510.1:n.66+35625dup (HSD11B1-AS1)
NM_005525.4:c.331+53dup (HSD11B1) MANE Select NP_005516.1:n.331+53dup
NM_001206741.2:c.331+53dup (HSD11B1) NP_001193670.1:n.331+53dup
NM_181755.3:c.331+53dup (HSD11B1) NP_861420.1:n.331+53dup