Canonical Allele Identifier: CA2738700729

Gene: AR

Linked Data

• dbSNP Id: rs2147497878

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686102del , CM000685.2:g.67686102del	GRCh38
NC_000023.10:g.66905944del , CM000685.1:g.66905944del	GRCh37
NC_000023.9:g.66822669del	NCBI36
NG_009014.2:g.147071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*209del	ENSP00000379358.4:n.*209del
ENST00000374690.9:c.1861del MANE Select	ENSP00000363822.3:p.Tyr621MetfsTer5
ENST00000396043.3:c.488del	ENSP00000379358.3:n.488del
ENST00000396044.8:c.1861del	ENSP00000379359.3:p.Tyr621MetfsTer5
ENST00000612452.5:c.1861del	ENSP00000484033.2:p.Tyr621MetfsTer5
ENST00000374690.7:c.1861del	ENSP00000363822.3:p.Tyr621MetfsTer5
ENST00000396043.2:c.265del	ENSP00000379358.2:p.Tyr89MetfsTer5
ENST00000396044.7:c.1861del	ENSP00000379359.3:p.Tyr621MetfsTer5
ENST00000504326.5:c.1861del	ENSP00000421155.1:p.Tyr621MetfsTer5
ENST00000513847.5:n.2188del
ENST00000514029.5:c.*342del	ENSP00000425199.1:n.*342del
ENST00000612010.4:c.*213del	ENSP00000482407.1:n.*213del
ENST00000612452.4:c.1291del	ENSP00000484033.1:p.Tyr431MetfsTer5
ENST00000613054.2:c.*59del	ENSP00000479013.1:n.*59del
NM_000044.3:c.1861del	NP_000035.2:p.Tyr621MetfsTer5
NM_001011645.2:c.265del	NP_001011645.1:p.Tyr89MetfsTer5
NM_000044.4:c.1861del	NP_000035.2:p.Tyr621MetfsTer5
NM_001011645.3:c.265del	NP_001011645.1:p.Tyr89MetfsTer5
NM_001348061.1:c.1861del	NP_001334990.1:p.Tyr621MetfsTer5
NM_001348063.1:c.1861del	NP_001334992.1:p.Tyr621MetfsTer5
NM_001348064.1:c.*59del	NP_001334993.1:n.*59del
NM_000044.6:c.1861del MANE Select	NP_000035.2:p.Tyr621MetfsTer5