Canonical Allele Identifier: CA11100754

Gene: PID1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.229105082A>G , CM000664.2:g.229105082A>G	GRCh38
NC_000002.11:g.229969798A>G , CM000664.1:g.229969798A>G	GRCh37
NC_000002.10:g.229678042A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392055.8:c.177+50736T>C MANE Select	ENSP00000375908.3:n.177+50736T>C
ENST00000354069.6:c.276+50736T>C	ENSP00000283937.8:n.276+50736T>C
ENST00000392054.7:c.270+50736T>C	ENSP00000375907.3:n.270+50736T>C
ENST00000392055.7:c.177+50736T>C	ENSP00000375908.3:n.177+50736T>C
ENST00000409462.1:c.31-78974T>C	ENSP00000386826.1:n.31-78974T>C
ENST00000482518.6:n.356+50736T>C
ENST00000534952.1:c.*158+50736T>C	ENSP00000438228.1:n.*158+50736T>C
NM_001100818.1:c.177+50736T>C	NP_001094288.1:n.177+50736T>C
NM_017933.4:c.270+50736T>C	NP_060403.3:n.270+50736T>C
XM_011511384.1:c.276+50736T>C	XP_011509686.1:n.276+50736T>C
NM_001330156.1:c.276+50736T>C	NP_001317085.1:n.276+50736T>C
NM_001330157.1:c.31-78974T>C	NP_001317086.1:n.31-78974T>C
NM_001330158.1:c.135+50736T>C	NP_001317087.1:n.135+50736T>C
XM_017004404.1:c.441+50736T>C	XP_016859893.1:n.441+50736T>C
NM_001100818.2:c.177+50736T>C MANE Select	NP_001094288.1:n.177+50736T>C
NM_001330157.2:c.31-78974T>C	NP_001317086.1:n.31-78974T>C
NM_001330158.2:c.135+50736T>C	NP_001317087.1:n.135+50736T>C
NM_017933.5:c.270+50736T>C	NP_060403.3:n.270+50736T>C