Canonical Allele Identifier: CA413424426
Gene: AR HGNC NCBI

Linked Data

gnomAD v4: X-67545495-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545495T>C , CM000685.2:g.67545495T>C GRCh38
NC_000023.10:g.66765337T>C , CM000685.1:g.66765337T>C GRCh37
NC_000023.9:g.66682062T>C NCBI36
NG_009014.2:g.6464T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.349T>C ENSP00000379358.4:p.Ser117Pro
ENST00000374690.9:c.349T>C MANE Select ENSP00000363822.3:p.Ser117Pro
ENST00000396044.8:c.349T>C ENSP00000379359.3:p.Ser117Pro
ENST00000612452.5:c.349T>C ENSP00000484033.2:p.Ser117Pro
ENST00000374690.7:c.349T>C ENSP00000363822.3:p.Ser117Pro
ENST00000396044.7:c.349T>C ENSP00000379359.3:p.Ser117Pro
ENST00000504326.5:c.349T>C ENSP00000421155.1:p.Ser117Pro
ENST00000513847.5:n.676T>C
ENST00000514029.5:c.349T>C ENSP00000425199.1:p.Ser117Pro
ENST00000612010.4:c.349T>C ENSP00000482407.1:p.Ser117Pro
ENST00000612452.4:c.-222T>C ENSP00000484033.1:n.-222T>C
ENST00000613054.2:c.349T>C ENSP00000479013.1:p.Ser117Pro
NM_000044.3:c.349T>C NP_000035.2:p.Ser117Pro
NM_000044.4:c.349T>C NP_000035.2:p.Ser117Pro
NM_001011645.3:c.-1435T>C NP_001011645.1:n.-1435T>C
NM_001348061.1:c.349T>C NP_001334990.1:p.Ser117Pro
NM_001348063.1:c.349T>C NP_001334992.1:p.Ser117Pro
NM_001348064.1:c.349T>C NP_001334993.1:p.Ser117Pro
NM_000044.6:c.349T>C MANE Select NP_000035.2:p.Ser117Pro