Canonical Allele Identifier: CA367001283

Gene: CRPPA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16278163T>C , CM000669.2:g.16278163T>C	GRCh38
NC_000007.13:g.16317788T>C , CM000669.1:g.16317788T>C	GRCh37
NC_000007.12:g.16284313T>C	NCBI36
NG_032690.1:g.148160A>G
NG_032690.2:g.148160A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407010.7:c.899A>G MANE Select	ENSP00000385478.2:p.His300Arg
ENST00000674759.1:c.596A>G	ENSP00000502749.1:p.His199Arg
ENST00000675257.1:c.491A>G	ENSP00000501664.1:p.His164Arg
ENST00000676325.1:c.596A>G	ENSP00000502074.1:p.His199Arg
ENST00000399310.3:c.749A>G	ENSP00000382249.3:p.His250Arg
ENST00000407010.6:c.899A>G	ENSP00000385478.2:p.His300Arg
ENST00000479493.1:n.110A>G
NM_001101417.3:c.749A>G	NP_001094887.1:p.His250Arg
NM_001101426.3:c.899A>G	NP_001094896.1:p.His300Arg
XM_006715770.2:c.650A>G	XP_006715833.1:p.His217Arg
XM_011515497.1:c.899A>G	XP_011513799.1:p.His300Arg
XM_011515498.1:c.899A>G	XP_011513800.1:p.His300Arg
XM_011515499.1:c.899A>G	XP_011513801.1:p.His300Arg
XM_011515500.1:c.794A>G	XP_011513802.1:p.His265Arg
XM_011515501.1:c.899A>G	XP_011513803.1:p.His300Arg
XM_011515502.1:c.596A>G	XP_011513804.1:p.His199Arg
XM_011515503.1:c.596A>G	XP_011513805.1:p.His199Arg
XM_011515504.1:c.596A>G	XP_011513806.1:p.His199Arg
XM_011515505.1:c.596A>G	XP_011513807.1:p.His199Arg
XM_011515506.1:c.596A>G	XP_011513808.1:p.His199Arg
XM_011515507.1:c.596A>G	XP_011513809.1:p.His199Arg
XM_011515508.1:c.596A>G	XP_011513810.1:p.His199Arg
XM_011515509.1:c.596A>G	XP_011513811.1:p.His199Arg
XM_006715770.3:c.650A>G	XP_006715833.1:p.His217Arg
XM_011515499.2:c.899A>G	XP_011513801.1:p.His300Arg
XM_011515500.2:c.794A>G	XP_011513802.1:p.His265Arg
XM_011515501.2:c.899A>G	XP_011513803.1:p.His300Arg
XM_011515508.2:c.596A>G	XP_011513810.1:p.His199Arg
XM_011515509.2:c.596A>G	XP_011513811.1:p.His199Arg
XM_017012575.1:c.899A>G	XP_016868064.1:p.His300Arg
XM_017012576.1:c.899A>G	XP_016868065.1:p.His300Arg
XM_017012577.1:c.263A>G	XP_016868066.1:p.His88Arg
XM_017012578.1:c.263A>G	XP_016868067.1:p.His88Arg
XM_024446909.1:c.596A>G	XP_024302677.1:p.His199Arg
XM_024446910.1:c.596A>G	XP_024302678.1:p.His199Arg
XM_024446911.1:c.491A>G	XP_024302679.1:p.His164Arg
XM_024446912.1:c.650A>G	XP_024302680.1:p.His217Arg
XR_001744864.1:n.1004A>G
XR_001744865.1:n.1012A>G
XR_001744866.1:n.1140A>G
XR_001744867.1:n.1098A>G
XR_001744868.1:n.907A>G
NM_001101426.4:c.899A>G MANE Select	NP_001094896.1:p.His300Arg
NM_001101417.4:c.749A>G	NP_001094887.1:p.His250Arg
NM_001368197.1:c.794A>G	NP_001355126.1:p.His265Arg
NR_160656.1:n.964A>G