Canonical Allele Identifier: CA2646921384

Gene: PSRC1

Linked Data

• gnomAD v4: 1-109279560-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109279560G>T , CM000663.2:g.109279560G>T	GRCh38
NC_000001.10:g.109822182G>T , CM000663.1:g.109822182G>T	GRCh37
NC_000001.9:g.109623705G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369909.7:c.*593C>A MANE Select	ENSP00000358925.2:n.*593C>A
ENST00000369904.7:c.*561C>A	ENSP00000358920.3:n.*561C>A
ENST00000369907.7:c.*593C>A	ENSP00000358923.3:n.*593C>A
ENST00000369909.6:c.*593C>A	ENSP00000358925.2:n.*593C>A
ENST00000409267.5:c.*593C>A	ENSP00000386323.1:n.*593C>A
NM_001005290.3:c.*561C>A	NP_001005290.1:n.*561C>A
NM_001032291.2:c.*593C>A	NP_001027462.1:n.*593C>A
NM_032636.7:c.*593C>A	NP_116025.1:n.*593C>A
XM_005271283.1:c.*593C>A	XP_005271340.1:n.*593C>A
XM_006710982.1:c.*593C>A	XP_006711045.1:n.*593C>A
XM_011542306.1:c.*593C>A	XP_011540608.1:n.*593C>A
NM_001350237.1:c.*593C>A	NP_001337166.1:n.*593C>A
NM_001350238.1:c.*593C>A	NP_001337167.1:n.*593C>A
NM_001350239.1:c.*593C>A	NP_001337168.1:n.*593C>A
NM_001350240.1:c.*593C>A	NP_001337169.1:n.*593C>A
NM_001350241.1:c.*593C>A	NP_001337170.1:n.*593C>A
NM_001350242.1:c.*593C>A	NP_001337171.1:n.*593C>A
NM_001363309.1:c.*593C>A	NP_001350238.1:n.*593C>A
XM_005271283.3:c.*593C>A	XP_005271340.1:n.*593C>A
XM_017002560.2:c.*593C>A	XP_016858049.1:n.*593C>A
XM_017002561.2:c.*593C>A	XP_016858050.1:n.*593C>A
XM_017002562.1:c.*593C>A	XP_016858051.1:n.*593C>A
XM_017002563.1:c.*593C>A	XP_016858052.1:n.*593C>A
XM_017002564.2:c.*593C>A	XP_016858053.1:n.*593C>A
XM_017002566.1:c.*593C>A	XP_016858055.1:n.*593C>A
XM_017002567.1:c.*593C>A	XP_016858056.1:n.*593C>A
XM_017002569.1:c.*593C>A	XP_016858058.1:n.*593C>A
XM_017002570.1:c.*593C>A	XP_016858059.1:n.*593C>A
XM_017002576.2:c.*561C>A	XP_016858065.1:n.*561C>A
XM_024450335.1:c.*593C>A	XP_024306103.1:n.*593C>A
XM_024450337.1:c.*561C>A	XP_024306105.1:n.*561C>A
XR_002957829.1:n.2044C>A
NM_001005290.4:c.*561C>A	NP_001005290.1:n.*561C>A
NM_001032291.3:c.*593C>A MANE Select	NP_001027462.1:n.*593C>A
NM_001350237.2:c.*593C>A	NP_001337166.1:n.*593C>A
NM_001350238.2:c.*593C>A	NP_001337167.1:n.*593C>A
NM_001350239.2:c.*593C>A	NP_001337168.1:n.*593C>A
NM_001350240.2:c.*593C>A	NP_001337169.1:n.*593C>A
NM_001350241.2:c.*593C>A	NP_001337170.1:n.*593C>A
NM_001350242.2:c.*593C>A	NP_001337171.1:n.*593C>A
NM_001363309.2:c.*593C>A	NP_001350238.1:n.*593C>A
NM_001394002.1:c.*593C>A	NP_001380931.1:n.*593C>A
NM_001394003.1:c.*561C>A	NP_001380932.1:n.*561C>A
NM_001394004.1:c.*561C>A	NP_001380933.1:n.*561C>A
NM_001394005.1:c.*593C>A	NP_001380934.1:n.*593C>A
NM_032636.8:c.*593C>A	NP_116025.1:n.*593C>A