Canonical Allele Identifier: CA7155041

Gene: PSMA6

Linked Data

• dbSNP Id: rs1048990
• ExAC: 14:35761675 C / T
• gnomAD v2: 14-35761675-C-T
• gnomAD v4: 14-35292469-C-T
• MyVariant Identifiers: chr14:g.35761675C>T (hg19) ; chr14:g.35292469C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35292469C>T , CM000676.2:g.35292469C>T	GRCh38
NC_000014.8:g.35761675C>T , CM000676.1:g.35761675C>T	GRCh37
NC_000014.7:g.34831426C>T	NCBI36
NG_011703.2:g.18912C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261479.9:c.-8C>T MANE Select	ENSP00000261479.4:n.-8C>T
ENST00000261479.8:c.-8C>T	ENSP00000261479.4:n.-8C>T
ENST00000540871.5:c.19+13751C>T	ENSP00000444844.1:n.19+13751C>T
ENST00000553688.5:c.-8C>T	ENSP00000450844.1:n.-8C>T
ENST00000553809.5:c.-8C>T	ENSP00000452603.1:n.-8C>T
ENST00000554541.5:c.-8C>T	ENSP00000451958.1:n.-8C>T
ENST00000554620.5:c.-8C>T	ENSP00000451432.1:n.-8C>T
ENST00000554843.5:n.82C>T
ENST00000554961.5:c.-8C>T	ENSP00000451254.1:n.-8C>T
ENST00000555764.5:c.-293C>T	ENSP00000452566.1:n.-293C>T
ENST00000556167.1:n.75C>T
ENST00000557565.1:c.*891+13751C>T	ENSP00000454657.1:n.*891+13751C>T
ENST00000622405.4:c.-150C>T	ENSP00000479620.1:n.-150C>T
ENST00000627895.2:c.-8C>T	ENSP00000485817.1:n.-8C>T
ENST00000628955.1:c.-8C>T	ENSP00000485776.1:n.-8C>T
NM_001282232.1:c.-293C>T	NP_001269161.1:n.-293C>T
NM_001282233.1:c.-150C>T	NP_001269162.1:n.-150C>T
NM_001282234.1:c.19+13751C>T	NP_001269163.1:n.19+13751C>T
NM_002791.2:c.-8C>T	NP_002782.1:n.-8C>T
NR_104110.1:n.153C>T
NM_002791.3:c.-8C>T MANE Select	NP_002782.1:n.-8C>T