Canonical Allele Identifier: CA367000405

Gene: CRPPA

Linked Data

• gnomAD v4: 7-16091779-C-A
• MyVariant Identifiers: chr7:g.16131404C>A (hg19) ; chr7:g.16091779C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16091779C>A , CM000669.2:g.16091779C>A	GRCh38
NC_000007.13:g.16131404C>A , CM000669.1:g.16131404C>A	GRCh37
NC_000007.12:g.16097929C>A	NCBI36
NG_032690.1:g.334544G>T
NG_032690.2:g.334544G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407010.7:c.1272G>T MANE Select	ENSP00000385478.2:p.Glu424Asp
ENST00000675257.1:c.864G>T	ENSP00000501664.1:p.Glu288Asp
ENST00000676325.1:c.969G>T	ENSP00000502074.1:p.Glu323Asp
ENST00000399310.3:c.1122G>T	ENSP00000382249.3:p.Glu374Asp
ENST00000407010.6:c.1272G>T	ENSP00000385478.2:p.Glu424Asp
NM_001101417.3:c.1122G>T	NP_001094887.1:p.Glu374Asp
NM_001101426.3:c.1272G>T	NP_001094896.1:p.Glu424Asp
XM_006715770.2:c.1023G>T	XP_006715833.1:p.Glu341Asp
XM_011515498.1:c.1251+124287G>T	XP_011513800.1:n.1251+124287G>T
XM_011515500.1:c.1167G>T	XP_011513802.1:p.Glu389Asp
XM_011515502.1:c.969G>T	XP_011513804.1:p.Glu323Asp
XM_011515503.1:c.969G>T	XP_011513805.1:p.Glu323Asp
XM_011515504.1:c.969G>T	XP_011513806.1:p.Glu323Asp
XM_011515505.1:c.969G>T	XP_011513807.1:p.Glu323Asp
XM_011515506.1:c.969G>T	XP_011513808.1:p.Glu323Asp
XM_011515507.1:c.969G>T	XP_011513809.1:p.Glu323Asp
XM_011515508.1:c.969G>T	XP_011513810.1:p.Glu323Asp
XM_011515509.1:c.969G>T	XP_011513811.1:p.Glu323Asp
XM_006715770.3:c.1023G>T	XP_006715833.1:p.Glu341Asp
XM_011515500.2:c.1167G>T	XP_011513802.1:p.Glu389Asp
XM_011515508.2:c.969G>T	XP_011513810.1:p.Glu323Asp
XM_011515509.2:c.969G>T	XP_011513811.1:p.Glu323Asp
XM_017012577.1:c.636G>T	XP_016868066.1:p.Glu212Asp
XM_017012578.1:c.636G>T	XP_016868067.1:p.Glu212Asp
XM_024446909.1:c.969G>T	XP_024302677.1:p.Glu323Asp
XM_024446910.1:c.969G>T	XP_024302678.1:p.Glu323Asp
XM_024446911.1:c.864G>T	XP_024302679.1:p.Glu288Asp
XR_001744868.1:n.1280G>T
NM_001101426.4:c.1272G>T MANE Select	NP_001094896.1:p.Glu424Asp
NM_001101417.4:c.1122G>T	NP_001094887.1:p.Glu374Asp
NM_001368197.1:c.1167G>T	NP_001355126.1:p.Glu389Asp
NR_160656.1:n.1337G>T