Canonical Allele Identifier: CA2693950092

Gene: AR

Linked Data

• gnomAD v4: X-67711748-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711748T>C , CM000685.2:g.67711748T>C	GRCh38
NC_000023.10:g.66931590T>C , CM000685.1:g.66931590T>C	GRCh37
NC_000023.9:g.66848315T>C	NCBI36
NG_009014.2:g.172717T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*521+59T>C	ENSP00000379358.4:n.*521+59T>C
ENST00000374690.9:c.2173+59T>C MANE Select	ENSP00000363822.3:n.2173+59T>C
ENST00000396043.3:c.800+59T>C	ENSP00000379358.3:n.800+59T>C
ENST00000396044.8:c.2173+59T>C	ENSP00000379359.3:n.2173+59T>C
ENST00000612452.5:c.2173+59T>C	ENSP00000484033.2:n.2173+59T>C
ENST00000374690.7:c.2173+59T>C	ENSP00000363822.3:n.2173+59T>C
ENST00000396043.2:c.577+59T>C	ENSP00000379358.2:n.577+59T>C
ENST00000396044.7:c.2173+59T>C	ENSP00000379359.3:n.2173+59T>C
ENST00000612452.4:c.1603+59T>C	ENSP00000484033.1:n.1603+59T>C
NM_000044.3:c.2173+59T>C	NP_000035.2:n.2173+59T>C
NM_001011645.2:c.577+59T>C	NP_001011645.1:n.577+59T>C
NM_000044.4:c.2173+59T>C	NP_000035.2:n.2173+59T>C
NM_001011645.3:c.577+59T>C	NP_001011645.1:n.577+59T>C
NM_000044.6:c.2173+59T>C MANE Select	NP_000035.2:n.2173+59T>C