Canonical Allele Identifier: CA2625041149

Gene: PSMA3 ARMH4

Linked Data

• gnomAD v4: 14-58263917-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58263917T>G , CM000676.2:g.58263917T>G	GRCh38
NC_000014.8:g.58730635T>G , CM000676.1:g.58730635T>G	GRCh37
NC_000014.7:g.57800388T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216455.9:c.543+147T>G (PSMA3) MANE Select	ENSP00000216455.4:n.543+147T>G
ENST00000216455.8:c.543+147T>G (PSMA3)	ENSP00000216455.4:n.543+147T>G
ENST00000412908.6:c.522+147T>G (PSMA3)	ENSP00000390491.2:n.522+147T>G
ENST00000553677.1:c.74+5919T>G (PSMA3)	ENSP00000450573.1:n.74+5919T>G
ENST00000554207.1:n.247+147T>G (PSMA3)
ENST00000554218.1:n.258+27718A>C (ARMH4)
ENST00000554812.5:n.613+147T>G (PSMA3)
ENST00000555743.1:n.585+147T>G (PSMA3)
ENST00000555931.5:c.*362+147T>G (PSMA3)	ENSP00000452437.1:n.*362+147T>G
ENST00000557087.5:c.*308+147T>G (PSMA3)	ENSP00000451461.1:n.*308+147T>G
ENST00000557508.5:c.318+147T>G (PSMA3)	ENSP00000452056.1:n.318+147T>G
NM_002788.3:c.543+147T>G (PSMA3)	NP_002779.1:n.543+147T>G
NM_152132.2:c.522+147T>G (PSMA3)	NP_687033.1:n.522+147T>G
NR_038123.1:n.576+147T>G (PSMA3)
NM_002788.4:c.543+147T>G (PSMA3) MANE Select	NP_002779.1:n.543+147T>G
NM_152132.3:c.522+147T>G (PSMA3)	NP_687033.1:n.522+147T>G
NR_038123.2:n.538+147T>G (PSMA3)