Canonical Allele Identifier: CA261603616

Gene: PSMA3 ARMH4

Linked Data

• dbSNP Id: rs113470609
• gnomAD v2: 14-58730644-T-TA
• gnomAD v3: 14-58263926-T-TA
• gnomAD v4: 14-58263926-T-TA
• MyVariant Identifiers: chr14:g.58730645_58730646insA (hg19) ; chr14:g.58730644_58730645insA (hg19) ; chr14:g.58263927_58263928insA (hg38) ; chr14:g.58263926_58263927insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58263935dup , CM000676.2:g.58263935dup	GRCh38
NC_000014.8:g.58730653dup , CM000676.1:g.58730653dup	GRCh37
NC_000014.7:g.57800406dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216455.9:c.543+165dup (PSMA3) MANE Select	ENSP00000216455.4:n.543+165dup
ENST00000216455.8:c.543+165dup (PSMA3)	ENSP00000216455.4:n.543+165dup
ENST00000412908.6:c.522+165dup (PSMA3)	ENSP00000390491.2:n.522+165dup
ENST00000553677.1:c.74+5937dup (PSMA3)	ENSP00000450573.1:n.74+5937dup
ENST00000554207.1:n.247+165dup (PSMA3)
ENST00000554218.1:n.258+27708dup (ARMH4)
ENST00000554812.5:n.613+165dup (PSMA3)
ENST00000555743.1:n.585+165dup (PSMA3)
ENST00000555931.5:c.*362+165dup (PSMA3)	ENSP00000452437.1:n.*362+165dup
ENST00000557087.5:c.*308+165dup (PSMA3)	ENSP00000451461.1:n.*308+165dup
ENST00000557508.5:c.318+165dup (PSMA3)	ENSP00000452056.1:n.318+165dup
NM_002788.3:c.543+165dup (PSMA3)	NP_002779.1:n.543+165dup
NM_152132.2:c.522+165dup (PSMA3)	NP_687033.1:n.522+165dup
NR_038123.1:n.576+165dup (PSMA3)
NM_002788.4:c.543+165dup (PSMA3) MANE Select	NP_002779.1:n.543+165dup
NM_152132.3:c.522+165dup (PSMA3)	NP_687033.1:n.522+165dup
NR_038123.2:n.538+165dup (PSMA3)