Canonical Allele Identifier: CA13993032

Linked Data

dbSNP Id: rs2348071

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58263908A>G , CM000676.2:g.58263908A>G GRCh38
NC_000014.8:g.58730626A>G , CM000676.1:g.58730626A>G GRCh37
NC_000014.7:g.57800379A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216455.9:c.543+138A>G (PSMA3) MANE Select ENSP00000216455.4:n.543+138A>G
ENST00000216455.8:c.543+138A>G (PSMA3) ENSP00000216455.4:n.543+138A>G
ENST00000412908.6:c.522+138A>G (PSMA3) ENSP00000390491.2:n.522+138A>G
ENST00000553677.1:c.74+5910A>G (PSMA3) ENSP00000450573.1:n.74+5910A>G
ENST00000554207.1:n.247+138A>G (PSMA3)
ENST00000554218.1:n.258+27727T>C (ARMH4)
ENST00000554812.5:n.613+138A>G (PSMA3)
ENST00000555743.1:n.585+138A>G (PSMA3)
ENST00000555931.5:c.*362+138A>G (PSMA3) ENSP00000452437.1:n.*362+138A>G
ENST00000557087.5:c.*308+138A>G (PSMA3) ENSP00000451461.1:n.*308+138A>G
ENST00000557508.5:c.318+138A>G (PSMA3) ENSP00000452056.1:n.318+138A>G
NM_002788.3:c.543+138A>G (PSMA3) NP_002779.1:n.543+138A>G
NM_152132.2:c.522+138A>G (PSMA3) NP_687033.1:n.522+138A>G
NR_038123.1:n.576+138A>G (PSMA3)
NM_002788.4:c.543+138A>G (PSMA3) MANE Select NP_002779.1:n.543+138A>G
NM_152132.3:c.522+138A>G (PSMA3) NP_687033.1:n.522+138A>G
NR_038123.2:n.538+138A>G (PSMA3)