Canonical Allele Identifier: CA573102088

Gene: CRPPA

Linked Data

• dbSNP Id: rs1242625031
• gnomAD v2: 7-16500229-G-C
• gnomAD v3: 7-16460604-G-C
• gnomAD v4: 7-16460604-G-C
• MyVariant Identifiers: chr7:g.16500229G>C (hg19) ; chr7:g.16460604G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16460604G>C , CM000669.2:g.16460604G>C	GRCh38
NC_000007.13:g.16500229G>C , CM000669.1:g.16500229G>C	GRCh37
NC_000007.12:g.16466754G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674759.1:c.-47+35776C>G	ENSP00000502749.1:n.-47+35776C>G
ENST00000675257.1:c.-47+35776C>G	ENSP00000501664.1:n.-47+35776C>G
XM_011515502.1:c.-47+35776C>G	XP_011513804.1:n.-47+35776C>G
XM_011515503.1:c.-47+35776C>G	XP_011513805.1:n.-47+35776C>G
XM_011515504.1:c.-47+35776C>G	XP_011513806.1:n.-47+35776C>G
XM_011515505.1:c.-47+35776C>G	XP_011513807.1:n.-47+35776C>G
XM_011515506.1:c.-47+35776C>G	XP_011513808.1:n.-47+35776C>G
XM_011515507.1:c.-47+35776C>G	XP_011513809.1:n.-47+35776C>G
XR_927059.1:n.405G>C
XM_024446909.1:c.-47+35776C>G	XP_024302677.1:n.-47+35776C>G
XM_024446910.1:c.-47+35776C>G	XP_024302678.1:n.-47+35776C>G
XM_024446911.1:c.-47+35776C>G	XP_024302679.1:n.-47+35776C>G