Canonical Allele Identifier: CA2035886790

Gene: CSRNP2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51073653G>T , CM000674.2:g.51073653G>T	GRCh38
NC_000012.11:g.51467436G>T , CM000674.1:g.51467436G>T	GRCh37
NC_000012.10:g.49753703G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228515.6:c.411+170C>A MANE Select	ENSP00000228515.1:n.411+170C>A
ENST00000228515.5:c.411+170C>A	ENSP00000228515.1:n.411+170C>A
ENST00000548206.1:c.129+170C>A	ENSP00000447983.1:n.129+170C>A
NM_030809.2:c.411+170C>A	NP_110436.1:n.411+170C>A
NR_045072.1:n.923+170C>A
XM_006719621.2:c.411+170C>A	XP_006719684.1:n.411+170C>A
XM_006719622.2:c.411+170C>A	XP_006719685.1:n.411+170C>A
XM_006719621.3:c.411+170C>A	XP_006719684.1:n.411+170C>A
XM_024449210.1:c.411+170C>A	XP_024304978.1:n.411+170C>A
XM_024449211.1:c.411+170C>A	XP_024304979.1:n.411+170C>A
XM_024449212.1:c.411+170C>A	XP_024304980.1:n.411+170C>A
XM_024449213.1:c.411+170C>A	XP_024304981.1:n.411+170C>A
XM_024449214.1:c.411+170C>A	XP_024304982.1:n.411+170C>A
XM_024449215.1:c.411+170C>A	XP_024304983.1:n.411+170C>A
XM_024449216.1:c.411+170C>A	XP_024304984.1:n.411+170C>A
NM_030809.3:c.411+170C>A MANE Select	NP_110436.1:n.411+170C>A
NR_045072.2:n.865+170C>A