Canonical Allele Identifier: CA173194999

Gene: PSD3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18789828G>A , CM000670.2:g.18789828G>A	GRCh38
NC_000008.10:g.18647338G>A , CM000670.1:g.18647338G>A	GRCh37
NC_000008.9:g.18691618G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327040.13:c.2082+9467C>T MANE Select	ENSP00000324127.8:n.2082+9467C>T
ENST00000286485.12:c.480+9467C>T	ENSP00000286485.8:n.480+9467C>T
ENST00000327040.12:c.2082+9467C>T	ENSP00000324127.8:n.2082+9467C>T
ENST00000440756.4:c.2086+9463C>T	ENSP00000401704.3:n.2086+9463C>T
ENST00000518315.5:c.480+9467C>T	ENSP00000428889.1:n.480+9467C>T
ENST00000519653.5:n.558-2994C>T
ENST00000519851.5:c.405+9467C>T	ENSP00000429069.1:n.405+9467C>T
ENST00000520858.5:c.379+9467C>T
ENST00000523619.5:c.1887+9467C>T	ENSP00000430640.1:n.1887+9467C>T
NM_015310.3:c.2082+9467C>T	NP_056125.3:n.2082+9467C>T
NM_206909.2:c.480+9467C>T	NP_996792.1:n.480+9467C>T
XM_011544462.1:c.2814+9467C>T	XP_011542764.1:n.2814+9467C>T
XM_011544463.1:c.2121+9467C>T	XP_011542765.1:n.2121+9467C>T
XM_011544464.1:c.2082+9467C>T	XP_011542766.1:n.2082+9467C>T
XM_011544465.1:c.2079+9467C>T	XP_011542767.1:n.2079+9467C>T
XM_011544466.1:c.1887+9467C>T	XP_011542768.1:n.1887+9467C>T
XM_011544467.1:c.2814+9467C>T	XP_011542769.1:n.2814+9467C>T
XM_011544468.1:c.2814+9467C>T	XP_011542770.1:n.2814+9467C>T
XM_011544469.1:c.2814+9467C>T	XP_011542771.1:n.2814+9467C>T
XM_011544470.1:c.1887+9467C>T	XP_011542772.1:n.1887+9467C>T
XM_011544471.1:c.2814+9467C>T	XP_011542773.1:n.2814+9467C>T
XM_011544472.1:c.2814+9467C>T	XP_011542774.1:n.2814+9467C>T
XM_011544473.1:c.2814+9467C>T	XP_011542775.1:n.2814+9467C>T
XM_011544474.1:c.480+9467C>T	XP_011542776.1:n.480+9467C>T
XM_011544475.1:c.405+9467C>T	XP_011542777.1:n.405+9467C>T
XM_011544476.1:c.405+9467C>T	XP_011542778.1:n.405+9467C>T
XR_949388.1:n.3032+9467C>T
NM_001362819.1:c.1983+9467C>T	NP_001349748.1:n.1983+9467C>T
XM_011544467.2:c.2814+9467C>T	XP_011542769.1:n.2814+9467C>T
XM_011544468.2:c.2814+9467C>T	XP_011542770.1:n.2814+9467C>T
XM_011544469.2:c.2814+9467C>T	XP_011542771.1:n.2814+9467C>T
XM_011544471.2:c.2814+9467C>T	XP_011542773.1:n.2814+9467C>T
XM_011544473.2:c.2814+9467C>T	XP_011542775.1:n.2814+9467C>T
XM_017013258.1:c.2142+9467C>T	XP_016868747.1:n.2142+9467C>T
XM_017013259.1:c.2121+9467C>T	XP_016868748.1:n.2121+9467C>T
XM_017013260.1:c.2079+9467C>T	XP_016868749.1:n.2079+9467C>T
XM_017013262.1:c.2814+9467C>T	XP_016868751.1:n.2814+9467C>T
XM_017013263.1:c.2814+9467C>T	XP_016868752.1:n.2814+9467C>T
XM_017013264.1:c.2082+9467C>T	XP_016868753.1:n.2082+9467C>T
XM_017013265.1:c.474+9467C>T	XP_016868754.1:n.474+9467C>T
XM_024447113.1:c.1887+9467C>T	XP_024302881.1:n.1887+9467C>T
NM_015310.4:c.2082+9467C>T MANE Select	NP_056125.3:n.2082+9467C>T
NM_001362819.2:c.1983+9467C>T	NP_001349748.1:n.1983+9467C>T
NM_206909.3:c.480+9467C>T	NP_996792.1:n.480+9467C>T