Canonical Allele Identifier: CA2693923888

Gene: AR

Linked Data

• gnomAD v4: X-67545004-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545004C>T , CM000685.2:g.67545004C>T	GRCh38
NC_000023.10:g.66764846C>T , CM000685.1:g.66764846C>T	GRCh37
NC_000023.9:g.66681571C>T	NCBI36
NG_009014.2:g.5973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.-143C>T	ENSP00000379358.4:n.-143C>T
ENST00000374690.9:c.-143C>T MANE Select	ENSP00000363822.3:n.-143C>T
ENST00000612452.5:c.-143C>T	ENSP00000484033.2:n.-143C>T
ENST00000374690.7:c.-143C>T	ENSP00000363822.3:n.-143C>T
ENST00000396044.7:c.-143C>T	ENSP00000379359.3:n.-143C>T
ENST00000504326.5:c.-143C>T	ENSP00000421155.1:n.-143C>T
ENST00000513847.5:n.185C>T
ENST00000514029.5:c.-143C>T	ENSP00000425199.1:n.-143C>T
ENST00000612010.4:c.-143C>T	ENSP00000482407.1:n.-143C>T
ENST00000612452.4:c.-713C>T	ENSP00000484033.1:n.-713C>T
ENST00000613054.2:c.-143C>T	ENSP00000479013.1:n.-143C>T
NM_000044.3:c.-143C>T	NP_000035.2:n.-143C>T
NM_000044.4:c.-143C>T	NP_000035.2:n.-143C>T
NM_001011645.3:c.-1926C>T	NP_001011645.1:n.-1926C>T
NM_001348061.1:c.-143C>T	NP_001334990.1:n.-143C>T
NM_001348063.1:c.-143C>T	NP_001334992.1:n.-143C>T
NM_001348064.1:c.-143C>T	NP_001334993.1:n.-143C>T
NM_000044.6:c.-143C>T MANE Select	NP_000035.2:n.-143C>T