Canonical Allele Identifier: CA413422656

Gene: AR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643284C>A , CM000685.2:g.67643284C>A	GRCh38
NC_000023.10:g.66863126C>A , CM000685.1:g.66863126C>A	GRCh37
NC_000023.9:g.66779851C>A	NCBI36
NG_009014.2:g.104253C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.1832C>A	ENSP00000379358.4:p.Ala611Asp
ENST00000374690.9:c.1645C>A MANE Select	ENSP00000363822.3:p.Pro549Thr
ENST00000396043.3:c.272C>A	ENSP00000379358.3:p.Ala91Asp
ENST00000396044.8:c.1645C>A	ENSP00000379359.3:p.Pro549Thr
ENST00000612452.5:c.1645C>A	ENSP00000484033.2:p.Pro549Thr
ENST00000374690.7:c.1645C>A	ENSP00000363822.3:p.Pro549Thr
ENST00000396043.2:c.49C>A	ENSP00000379358.2:p.Pro17Thr
ENST00000396044.7:c.1645C>A	ENSP00000379359.3:p.Pro549Thr
ENST00000504326.5:c.1645C>A	ENSP00000421155.1:p.Pro549Thr
ENST00000513847.5:n.1972C>A
ENST00000514029.5:c.1645C>A	ENSP00000425199.1:p.Pro549Thr
ENST00000612010.4:c.1645C>A	ENSP00000482407.1:p.Pro549Thr
ENST00000612452.4:c.1075C>A	ENSP00000484033.1:p.Pro359Thr
ENST00000613054.2:c.1617-42657C>A	ENSP00000479013.1:n.1617-42657C>A
NM_000044.3:c.1645C>A	NP_000035.2:p.Pro549Thr
NM_001011645.2:c.49C>A	NP_001011645.1:p.Pro17Thr
NM_000044.4:c.1645C>A	NP_000035.2:p.Pro549Thr
NM_001011645.3:c.49C>A	NP_001011645.1:p.Pro17Thr
NM_001348061.1:c.1645C>A	NP_001334990.1:p.Pro549Thr
NM_001348063.1:c.1645C>A	NP_001334992.1:p.Pro549Thr
NM_001348064.1:c.1617-42657C>A	NP_001334993.1:n.1617-42657C>A
NM_000044.6:c.1645C>A MANE Select	NP_000035.2:p.Pro549Thr