Canonical Allele Identifier: CA1789659743

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64604838_64604839delinsAG , CM000670.2:g.64604838_64604839delinsAG	GRCh38
NC_000008.10:g.65517395_65517396delinsAG , CM000670.1:g.65517395_65517396delinsAG	GRCh37
NC_000008.9:g.65679949_65679950delinsAG	NCBI36
NG_008338.1:g.198953_198954delinsCT
NG_008338.2:g.198953_198954delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.1076_1077delinsCT MANE Select	ENSP00000310721.3:p.Ala359=
ENST00000310193.3:c.1076_1077delinsCT	ENSP00000310721.3:p.Ala359=
ENST00000523954.1:n.350_351delinsCT
NM_004820.3:c.1076_1077delinsCT	NP_004811.1:p.Ala359=
NM_001324112.1:c.1076_1077delinsCT	NP_001311041.1:p.Ala359=
NM_004820.4:c.1076_1077delinsCT	NP_004811.1:p.Ala359=
XM_017014002.1:c.1142_1143delinsCT	XP_016869491.1:p.Ala381=
NM_004820.5:c.1076_1077delinsCT MANE Select	NP_004811.1:p.Ala359=
NM_001324112.2:c.1076_1077delinsCT	NP_001311041.1:p.Ala359=