Canonical Allele Identifier: CA16510569

Gene: PSMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78540881A>C , CM000677.2:g.78540881A>C	GRCh38
NC_000015.9:g.78833223A>C , CM000677.1:g.78833223A>C	GRCh37
NC_000015.8:g.76620278A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002789.6:c.-24+342A>C MANE Select	NP_002780.1:n.-24+342A>C
ENST00000044462.12:c.-24+342A>C MANE Select	ENSP00000044462.7:n.-24+342A>C
NM_001102667.1:c.-24+418A>C	NP_001096137.1:n.-24+418A>C
NM_001102667.2:c.-24+418A>C	NP_001096137.1:n.-24+418A>C
NM_001102668.1:c.-74+342A>C	NP_001096138.1:n.-74+342A>C
NM_001102668.2:c.-74+342A>C	NP_001096138.1:n.-74+342A>C
NM_001102668.3:c.-74+342A>C	NP_001096138.1:n.-74+342A>C
NM_001330673.1:c.-24+342A>C	NP_001317602.1:n.-24+342A>C
NM_001330673.2:c.-24+342A>C	NP_001317602.1:n.-24+342A>C
NM_001330675.1:c.-24+342A>C	NP_001317604.1:n.-24+342A>C
NM_001330675.2:c.-24+342A>C	NP_001317604.1:n.-24+342A>C
NM_001330676.1:c.-24+46A>C	NP_001317605.1:n.-24+46A>C
NM_001330676.2:c.-24+46A>C	NP_001317605.1:n.-24+46A>C
NM_002789.4:c.-24+342A>C	NP_002780.1:n.-24+342A>C
NM_002789.5:c.-24+342A>C	NP_002780.1:n.-24+342A>C
ENST00000044462.11:c.-24+342A>C	ENSP00000044462.7:n.-24+342A>C
ENST00000413382.6:c.-74+342A>C	ENSP00000402118.2:n.-74+342A>C
ENST00000557929.5:n.73+342A>C
ENST00000558281.5:c.-24+342A>C	ENSP00000453145.1:n.-24+342A>C
ENST00000558341.5:c.-24+46A>C	ENSP00000453323.1:n.-24+46A>C
ENST00000558635.1:n.81+342A>C
ENST00000558639.5:n.96+342A>C
ENST00000559082.5:c.-24+418A>C	ENSP00000453887.1:n.-24+418A>C
ENST00000559146.5:c.-24+342A>C	ENSP00000453621.1:n.-24+342A>C
ENST00000559365.5:c.-24+46A>C	ENSP00000453802.1:n.-24+46A>C
ENST00000559437.5:c.-93A>C	ENSP00000453523.1:n.-93A>C
ENST00000559934.5:n.438A>C
ENST00000559948.5:c.-53+342A>C	ENSP00000452936.1:n.-53+342A>C
ENST00000560033.5:n.37+418A>C
ENST00000560099.5:n.421A>C
ENST00000560217.5:c.-24+342A>C	ENSP00000453829.1:n.-24+342A>C