Canonical Allele Identifier: CA2693923852

Gene: AR

Linked Data

• gnomAD v4: X-67544971-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67544971G>T , CM000685.2:g.67544971G>T	GRCh38
NC_000023.10:g.66764813G>T , CM000685.1:g.66764813G>T	GRCh37
NC_000023.9:g.66681538G>T	NCBI36
NG_009014.2:g.5940G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.-176G>T	ENSP00000379358.4:n.-176G>T
ENST00000374690.9:c.-176G>T MANE Select	ENSP00000363822.3:n.-176G>T
ENST00000612452.5:c.-176G>T	ENSP00000484033.2:n.-176G>T
ENST00000374690.7:c.-176G>T	ENSP00000363822.3:n.-176G>T
ENST00000396044.7:c.-176G>T	ENSP00000379359.3:n.-176G>T
ENST00000504326.5:c.-176G>T	ENSP00000421155.1:n.-176G>T
ENST00000513847.5:n.152G>T
ENST00000514029.5:c.-176G>T	ENSP00000425199.1:n.-176G>T
ENST00000612010.4:c.-176G>T	ENSP00000482407.1:n.-176G>T
ENST00000612452.4:c.-746G>T	ENSP00000484033.1:n.-746G>T
ENST00000613054.2:c.-176G>T	ENSP00000479013.1:n.-176G>T
NM_000044.3:c.-176G>T	NP_000035.2:n.-176G>T
NM_000044.4:c.-176G>T	NP_000035.2:n.-176G>T
NM_001011645.3:c.-1959G>T	NP_001011645.1:n.-1959G>T
NM_001348061.1:c.-176G>T	NP_001334990.1:n.-176G>T
NM_001348063.1:c.-176G>T	NP_001334992.1:n.-176G>T
NM_001348064.1:c.-176G>T	NP_001334993.1:n.-176G>T
NM_000044.6:c.-176G>T MANE Select	NP_000035.2:n.-176G>T