Canonical Allele Identifier: CA14121451

Gene: PPCDC

Linked Data

• dbSNP Id: rs1867148
• gnomAD v2: 15-75339985-T-C
• gnomAD v3: 15-75047644-T-C
• gnomAD v4: 15-75047644-T-C
• MyVariant Identifiers: chr15:g.75339985T>C (hg19) ; chr15:g.75047644T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.75047644T>C , CM000677.2:g.75047644T>C	GRCh38
NC_000015.9:g.75339985T>C , CM000677.1:g.75339985T>C	GRCh37
NC_000015.8:g.73127038T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000342932.8:c.361-909T>C MANE Select	ENSP00000343190.3:n.361-909T>C
ENST00000342932.7:c.361-909T>C	ENSP00000343190.3:n.361-909T>C
ENST00000563393.1:c.-9-909T>C	ENSP00000457490.1:n.-9-909T>C
ENST00000564923.5:c.136-909T>C	ENSP00000456665.1:n.136-909T>C
ENST00000567336.1:c.265-909T>C	ENSP00000456353.1:n.265-909T>C
ENST00000568649.5:c.232-909T>C	ENSP00000455691.1:n.232-909T>C
ENST00000569562.5:c.-9-909T>C	ENSP00000455499.1:n.-9-909T>C
NM_001301101.1:c.232-909T>C	NP_001288030.1:n.232-909T>C
NM_001301102.1:c.265-909T>C	NP_001288031.1:n.265-909T>C
NM_001301103.1:c.136-909T>C	NP_001288032.1:n.136-909T>C
NM_001301104.1:c.-9-909T>C	NP_001288033.1:n.-9-909T>C
NM_001301105.1:c.-9-909T>C	NP_001288034.1:n.-9-909T>C
NM_021823.4:c.361-909T>C	NP_068595.3:n.361-909T>C
NR_125369.1:n.298-909T>C
XM_017022461.1:c.265-909T>C	XP_016877950.1:n.265-909T>C
XM_017022462.1:c.190-909T>C	XP_016877951.1:n.190-909T>C
XM_017022463.2:c.-112T>C	XP_016877952.1:n.-112T>C
XM_017022464.1:c.136-909T>C	XP_016877953.1:n.136-909T>C
XM_017022465.2:c.361-909T>C	XP_016877954.1:n.361-909T>C
NM_021823.5:c.361-909T>C MANE Select	NP_068595.3:n.361-909T>C
NM_001301101.2:c.232-909T>C	NP_001288030.1:n.232-909T>C
NM_001301102.2:c.265-909T>C	NP_001288031.1:n.265-909T>C
NM_001301103.2:c.136-909T>C	NP_001288032.1:n.136-909T>C
NM_001301104.2:c.-9-909T>C	NP_001288033.1:n.-9-909T>C
NM_001301105.2:c.-9-909T>C	NP_001288034.1:n.-9-909T>C
NR_125369.2:n.263-909T>C