Canonical Allele Identifier: CA1777329091
Community Standard Title: NM_000025.3(ADRB3):c.638_641delinsTCTA (p.Phe213=)
Gene: ADRB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965829_37965832delinsTAGA , CM000670.2:g.37965829_37965832delinsTAGA GRCh38
NC_000008.10:g.37823347_37823350delinsTAGA , CM000670.1:g.37823347_37823350delinsTAGA GRCh37
NC_000008.9:g.37942504_37942507delinsTAGA NCBI36
NG_011936.1:g.5835_5838delinsTCTA

Transcript Alleles

HGVS Amino-acid Change
NM_000025.3:c.638_641delinsTCTA MANE Select NP_000016.1:p.Phe213=
ENST00000345060.5:c.638_641delinsTCTA MANE Select ENSP00000343782.3:p.Phe213=
NM_000025.2:c.638_641delinsTCTA NP_000016.1:p.Phe213=
ENST00000345060.4:c.638_641delinsTCTA ENSP00000343782.3:p.Phe213=
ENST00000520341.2:n.766_769delinsTCTA
ENST00000614635.1:c.638_641delinsTCTA ENSP00000480325.1:p.Phe213=
ENST00000647937.1:c.122_125delinsTCTA ENSP00000497740.1:p.Phe41=