Canonical Allele Identifier: CA2780623687

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624555_64624556insGA , CM000670.2:g.64624555_64624556insGA	GRCh38
NC_000008.10:g.65537112_65537113insGA , CM000670.1:g.65537112_65537113insGA	GRCh37
NC_000008.9:g.65699666_65699667insGA	NCBI36
NG_008338.1:g.179237_179238insCT
NG_008338.2:g.179237_179238insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.123-16_123-15insCT MANE Select	ENSP00000310721.3:n.123-16_123-15insCT
ENST00000310193.3:c.123-16_123-15insCT	ENSP00000310721.3:n.123-16_123-15insCT
NM_004820.3:c.123-16_123-15insCT	NP_004811.1:n.123-16_123-15insCT
NM_001324112.1:c.123-16_123-15insCT	NP_001311041.1:n.123-16_123-15insCT
NM_004820.4:c.123-16_123-15insCT	NP_004811.1:n.123-16_123-15insCT
XM_017014002.1:c.189-16_189-15insCT	XP_016869491.1:n.189-16_189-15insCT
NM_004820.5:c.123-16_123-15insCT MANE Select	NP_004811.1:n.123-16_123-15insCT
NM_001324112.2:c.123-16_123-15insCT	NP_001311041.1:n.123-16_123-15insCT