Canonical Allele Identifier: CA4169312

Gene: CRPPA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16091661G>C , CM000669.2:g.16091661G>C	GRCh38
NC_000007.13:g.16131286G>C , CM000669.1:g.16131286G>C	GRCh37
NC_000007.12:g.16097811G>C	NCBI36
NG_032690.1:g.334662C>G
NG_032690.2:g.334662C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001101426.4:c.*34C>G MANE Select	NP_001094896.1:n.*34C>G
ENST00000407010.7:c.*34C>G MANE Select	ENSP00000385478.2:n.*34C>G
NM_001101417.3:c.1240C>G	NP_001094887.1:n.1240C>G
NM_001101417.4:c.*34C>G	NP_001094887.1:n.*34C>G
NM_001101426.3:c.1390C>G	NP_001094896.1:n.1390C>G
NM_001368197.1:c.*34C>G	NP_001355126.1:n.*34C>G
NR_160656.1:n.1455C>G
ENST00000399310.3:c.1240C>G	ENSP00000382249.3:n.1240C>G
ENST00000407010.6:c.1390C>G	ENSP00000385478.2:n.1390C>G
ENST00000675257.1:c.*34C>G	ENSP00000501664.1:n.*34C>G
ENST00000676325.1:c.*34C>G	ENSP00000502074.1:n.*34C>G
XM_006715770.2:c.*34C>G	XP_006715833.1:n.*34C>G
XM_006715770.3:c.*34C>G	XP_006715833.1:n.*34C>G
XM_011515498.1:c.1251+124405C>G	XP_011513800.1:n.1251+124405C>G
XM_011515500.1:c.*34C>G	XP_011513802.1:n.*34C>G
XM_011515500.2:c.*34C>G	XP_011513802.1:n.*34C>G
XM_011515502.1:c.*34C>G	XP_011513804.1:n.*34C>G
XM_011515503.1:c.*34C>G	XP_011513805.1:n.*34C>G
XM_011515504.1:c.*34C>G	XP_011513806.1:n.*34C>G
XM_011515505.1:c.*34C>G	XP_011513807.1:n.*34C>G
XM_011515506.1:c.*34C>G	XP_011513808.1:n.*34C>G
XM_011515507.1:c.*34C>G	XP_011513809.1:n.*34C>G
XM_011515508.1:c.*34C>G	XP_011513810.1:n.*34C>G
XM_011515508.2:c.*34C>G	XP_011513810.1:n.*34C>G
XM_011515509.1:c.*34C>G	XP_011513811.1:n.*34C>G
XM_011515509.2:c.*34C>G	XP_011513811.1:n.*34C>G
XM_017012577.1:c.*34C>G	XP_016868066.1:n.*34C>G
XM_017012578.1:c.*34C>G	XP_016868067.1:n.*34C>G
XM_024446909.1:c.*34C>G	XP_024302677.1:n.*34C>G
XM_024446910.1:c.*34C>G	XP_024302678.1:n.*34C>G
XM_024446911.1:c.*34C>G	XP_024302679.1:n.*34C>G
XR_001744868.1:n.1398C>G