Canonical Allele Identifier: CA1789668054
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624547_64624549delinsGAA , CM000670.2:g.64624547_64624549delinsGAA GRCh38
NC_000008.10:g.65537104_65537106delinsGAA , CM000670.1:g.65537104_65537106delinsGAA GRCh37
NC_000008.9:g.65699658_65699660delinsGAA NCBI36
NG_008338.1:g.179243_179245delinsTTC
NG_008338.2:g.179243_179245delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.123-10_123-8delinsTTC MANE Select ENSP00000310721.3:n.123-10_123-8delinsTTC
ENST00000310193.3:c.123-10_123-8delinsTTC ENSP00000310721.3:n.123-10_123-8delinsTTC
NM_004820.3:c.123-10_123-8delinsTTC NP_004811.1:n.123-10_123-8delinsTTC
NM_001324112.1:c.123-10_123-8delinsTTC NP_001311041.1:n.123-10_123-8delinsTTC
NM_004820.4:c.123-10_123-8delinsTTC NP_004811.1:n.123-10_123-8delinsTTC
XM_017014002.1:c.189-10_189-8delinsTTC XP_016869491.1:n.189-10_189-8delinsTTC
NM_004820.5:c.123-10_123-8delinsTTC MANE Select NP_004811.1:n.123-10_123-8delinsTTC
NM_001324112.2:c.123-10_123-8delinsTTC NP_001311041.1:n.123-10_123-8delinsTTC