Canonical Allele Identifier: CA2484332166

Gene: HSD11B1 HSD11B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209707080A= , CM000663.2:g.209707080A=	GRCh38
NC_000001.10:g.209880425A= , CM000663.1:g.209880425A=	GRCh37
NC_000001.9:g.207947048A=	NCBI36
NG_012081.1:g.25876A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367027.5:c.469A= (HSD11B1) MANE Select	ENSP00000355994.3:p.Met157=
ENST00000261465.5:c.469A= (HSD11B1)	ENSP00000261465.2:p.Met157=
ENST00000367027.4:c.469A= (HSD11B1)	ENSP00000355994.3:p.Met157=
ENST00000367028.6:c.469A= (HSD11B1)	ENSP00000355995.1:p.Met157=
ENST00000615289.4:c.469A= (HSD11B1)	ENSP00000478430.1:p.Met157=
NM_001206741.1:c.469A= (HSD11B1)	NP_001193670.1:p.Met157=
NM_005525.3:c.469A= (HSD11B1)	NP_005516.1:p.Met157=
NM_181755.2:c.469A= (HSD11B1)	NP_861420.1:p.Met157=
XR_922542.1:n.3234+16950T= (HSD11B1-AS1)
XR_922543.1:n.3225+16950T= (HSD11B1-AS1)
XR_922547.1:n.3090+35417T= (HSD11B1-AS1)
XR_922549.1:n.125-44019T= (HSD11B1-AS1)
NR_134509.1:n.96+16950T= (HSD11B1-AS1)
NR_134510.1:n.66+35417T= (HSD11B1-AS1)
NM_005525.4:c.469A= (HSD11B1) MANE Select	NP_005516.1:p.Met157=
NM_001206741.2:c.469A= (HSD11B1)	NP_001193670.1:p.Met157=
NM_181755.3:c.469A= (HSD11B1)	NP_861420.1:p.Met157=