Canonical Allele Identifier: CA413428143

Gene: AR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723689G>C , CM000685.2:g.67723689G>C	GRCh38
NC_000023.10:g.66943531G>C , CM000685.1:g.66943531G>C	GRCh37
NC_000023.9:g.66860256G>C	NCBI36
NG_009014.2:g.184658G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*959G>C	ENSP00000379358.4:n.*959G>C
ENST00000374690.9:c.2611G>C MANE Select	ENSP00000363822.3:p.Ala871Pro
ENST00000396043.3:c.1238G>C	ENSP00000379358.3:n.1238G>C
ENST00000396044.8:c.2177G>C	ENSP00000379359.3:p.Cys726Ser
ENST00000612452.5:c.2611G>C	ENSP00000484033.2:p.Ala871Pro
ENST00000374690.7:c.2611G>C	ENSP00000363822.3:p.Ala871Pro
ENST00000396043.2:c.1015G>C	ENSP00000379358.2:p.Ala339Pro
ENST00000396044.7:c.2177G>C	ENSP00000379359.3:p.Cys726Ser
ENST00000612452.4:c.2062G>C	ENSP00000484033.1:p.Ala688Pro
NM_000044.3:c.2611G>C	NP_000035.2:p.Ala871Pro
NM_001011645.2:c.1015G>C	NP_001011645.1:p.Ala339Pro
NM_000044.4:c.2611G>C	NP_000035.2:p.Ala871Pro
NM_001011645.3:c.1015G>C	NP_001011645.1:p.Ala339Pro
NM_000044.6:c.2611G>C MANE Select	NP_000035.2:p.Ala871Pro