Canonical Allele Identifier: CA349164660

Gene: BBS5

Linked Data

• MyVariant Identifiers: chr2:g.170349412G>T (hg19) ; chr2:g.169492902G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169492902G>T , CM000664.2:g.169492902G>T	GRCh38
NC_000002.11:g.170349412G>T , CM000664.1:g.170349412G>T	GRCh37
NC_000002.10:g.170057658G>T	NCBI36
NG_011567.1:g.18407G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295240.8:c.415G>T MANE Select	ENSP00000295240.3:p.Asp139Tyr
ENST00000295240.7:c.415G>T	ENSP00000295240.3:p.Asp139Tyr
ENST00000392663.6:c.415G>T	ENSP00000376431.2:p.Asp139Tyr
ENST00000443151.1:c.*137G>T	ENSP00000406182.1:n.*137G>T
ENST00000475571.1:n.382G>T
ENST00000513963.1:c.415G>T	ENSP00000424363.1:p.Asp139Tyr
NM_152384.2:c.415G>T	NP_689597.1:p.Asp139Tyr
NM_152384.3:c.415G>T MANE Select	NP_689597.1:p.Asp139Tyr