Canonical Allele Identifier: CA367001768

Gene: CRPPA

Linked Data

• gnomAD v4: 7-16308619-G-C
• MyVariant Identifiers: chr7:g.16348244G>C (hg19) ; chr7:g.16308619G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16308619G>C , CM000669.2:g.16308619G>C	GRCh38
NC_000007.13:g.16348244G>C , CM000669.1:g.16348244G>C	GRCh37
NC_000007.12:g.16314769G>C	NCBI36
NG_032690.1:g.117704C>G
NG_032690.2:g.117704C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407010.7:c.693C>G MANE Select	ENSP00000385478.2:p.Asp231Glu
ENST00000674759.1:c.390C>G	ENSP00000502749.1:p.Asp130Glu
ENST00000675257.1:c.382-7153C>G	ENSP00000501664.1:n.382-7153C>G
ENST00000676325.1:c.390C>G	ENSP00000502074.1:p.Asp130Glu
ENST00000399310.3:c.543C>G	ENSP00000382249.3:p.Asp181Glu
ENST00000407010.6:c.693C>G	ENSP00000385478.2:p.Asp231Glu
NM_001101417.3:c.543C>G	NP_001094887.1:p.Asp181Glu
NM_001101426.3:c.693C>G	NP_001094896.1:p.Asp231Glu
XM_006715770.2:c.444C>G	XP_006715833.1:p.Asp148Glu
XM_011515497.1:c.693C>G	XP_011513799.1:p.Asp231Glu
XM_011515498.1:c.693C>G	XP_011513800.1:p.Asp231Glu
XM_011515499.1:c.693C>G	XP_011513801.1:p.Asp231Glu
XM_011515500.1:c.685-7153C>G	XP_011513802.1:n.685-7153C>G
XM_011515501.1:c.693C>G	XP_011513803.1:p.Asp231Glu
XM_011515502.1:c.390C>G	XP_011513804.1:p.Asp130Glu
XM_011515503.1:c.390C>G	XP_011513805.1:p.Asp130Glu
XM_011515504.1:c.390C>G	XP_011513806.1:p.Asp130Glu
XM_011515505.1:c.390C>G	XP_011513807.1:p.Asp130Glu
XM_011515506.1:c.390C>G	XP_011513808.1:p.Asp130Glu
XM_011515507.1:c.390C>G	XP_011513809.1:p.Asp130Glu
XM_011515508.1:c.390C>G	XP_011513810.1:p.Asp130Glu
XM_011515509.1:c.390C>G	XP_011513811.1:p.Asp130Glu
XM_011515511.1:c.685-30393C>G	XP_011513813.1:n.685-30393C>G
XM_006715770.3:c.444C>G	XP_006715833.1:p.Asp148Glu
XM_011515499.2:c.693C>G	XP_011513801.1:p.Asp231Glu
XM_011515500.2:c.685-7153C>G	XP_011513802.1:n.685-7153C>G
XM_011515501.2:c.693C>G	XP_011513803.1:p.Asp231Glu
XM_011515508.2:c.390C>G	XP_011513810.1:p.Asp130Glu
XM_011515509.2:c.390C>G	XP_011513811.1:p.Asp130Glu
XM_017012575.1:c.693C>G	XP_016868064.1:p.Asp231Glu
XM_017012576.1:c.693C>G	XP_016868065.1:p.Asp231Glu
XM_017012577.1:c.57C>G	XP_016868066.1:p.Asp19Glu
XM_017012578.1:c.57C>G	XP_016868067.1:p.Asp19Glu
XM_024446909.1:c.390C>G	XP_024302677.1:p.Asp130Glu
XM_024446910.1:c.390C>G	XP_024302678.1:p.Asp130Glu
XM_024446911.1:c.382-7153C>G	XP_024302679.1:n.382-7153C>G
XM_024446912.1:c.444C>G	XP_024302680.1:p.Asp148Glu
XR_001744864.1:n.844C>G
XR_001744865.1:n.852C>G
XR_001744866.1:n.934C>G
XR_001744867.1:n.938C>G
XR_001744868.1:n.844-30393C>G
NM_001101426.4:c.693C>G MANE Select	NP_001094896.1:p.Asp231Glu
NM_001101417.4:c.543C>G	NP_001094887.1:p.Asp181Glu
NM_001368197.1:c.685-7153C>G	NP_001355126.1:n.685-7153C>G
NR_160656.1:n.901-30393C>G