Canonical Allele Identifier: CA2780623691

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624575_64624576insCCCAAACACACCCAACAC , CM000670.2:g.64624575_64624576insCCCAAACACACCCAACAC	GRCh38
NC_000008.10:g.65537132_65537133insCCCAAACACACCCAACAC , CM000670.1:g.65537132_65537133insCCCAAACACACCCAACAC	GRCh37
NC_000008.9:g.65699686_65699687insCCCAAACACACCCAACAC	NCBI36
NG_008338.1:g.179216_179217insGTGTTGGGTGTGTTTGGG
NG_008338.2:g.179216_179217insGTGTTGGGTGTGTTTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.123-37_123-36insGTGTTGGGTGTGTTTGGG MANE Select	ENSP00000310721.3:n.123-37_123-36insGTGTTGGGTGTGTTTGGG
ENST00000310193.3:c.123-37_123-36insGTGTTGGGTGTGTTTGGG	ENSP00000310721.3:n.123-37_123-36insGTGTTGGGTGTGTTTGGG
NM_004820.3:c.123-37_123-36insGTGTTGGGTGTGTTTGGG	NP_004811.1:n.123-37_123-36insGTGTTGGGTGTGTTTGGG
NM_001324112.1:c.123-37_123-36insGTGTTGGGTGTGTTTGGG	NP_001311041.1:n.123-37_123-36insGTGTTGGGTGTGTTTGGG
NM_004820.4:c.123-37_123-36insGTGTTGGGTGTGTTTGGG	NP_004811.1:n.123-37_123-36insGTGTTGGGTGTGTTTGGG
XM_017014002.1:c.189-37_189-36insGTGTTGGGTGTGTTTGGG	XP_016869491.1:n.189-37_189-36insGTGTTGGGTGTGTTTGGG
NM_004820.5:c.123-37_123-36insGTGTTGGGTGTGTTTGGG MANE Select	NP_004811.1:n.123-37_123-36insGTGTTGGGTGTGTTTGGG
NM_001324112.2:c.123-37_123-36insGTGTTGGGTGTGTTTGGG	NP_001311041.1:n.123-37_123-36insGTGTTGGGTGTGTTTGGG