Canonical Allele Identifier: CA13214471

Gene: CELF2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.10958376G>T , CM000672.2:g.10958376G>T	GRCh38
NC_000010.10:g.11000339G>T , CM000672.1:g.11000339G>T	GRCh37
NC_000010.9:g.11040345G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636488.1:c.89+38377G>T	ENSP00000489955.1:n.89+38377G>T
ENST00000637215.1:c.89+38377G>T	ENSP00000490185.1:n.89+38377G>T
ENST00000638035.1:c.-20+38377G>T	ENSP00000490401.1:n.-20+38377G>T
NM_001326317.1:c.-20+38377G>T	NP_001313246.1:n.-20+38377G>T
NM_001326318.1:c.-20+38377G>T	NP_001313247.1:n.-20+38377G>T
NM_001326319.1:c.-20+17922G>T	NP_001313248.1:n.-20+17922G>T
NM_001326320.1:c.-20+38377G>T	NP_001313249.1:n.-20+38377G>T
NM_001326321.1:c.-20+38377G>T	NP_001313250.1:n.-20+38377G>T
NM_001326323.1:c.-20+38377G>T	NP_001313252.1:n.-20+38377G>T
NM_001326324.1:c.-20+38377G>T	NP_001313253.1:n.-20+38377G>T
NM_001326325.1:c.146+38377G>T	NP_001313254.1:n.146+38377G>T
NM_001326326.1:c.89+38377G>T	NP_001313255.1:n.89+38377G>T
NM_001326327.1:c.89+38377G>T	NP_001313256.1:n.89+38377G>T
NM_001326328.1:c.-20+38377G>T	NP_001313257.1:n.-20+38377G>T
XM_017015557.1:c.-198+38377G>T	XP_016871046.1:n.-198+38377G>T
XM_017015568.2:c.-552+38377G>T	XP_016871057.1:n.-552+38377G>T
XM_024447772.1:c.146+38377G>T	XP_024303540.1:n.146+38377G>T
XM_024447773.1:c.89+38377G>T	XP_024303541.1:n.89+38377G>T
XM_024447774.1:c.89+38377G>T	XP_024303542.1:n.89+38377G>T
XM_024447775.1:c.89+38377G>T	XP_024303543.1:n.89+38377G>T
NM_001326317.2:c.-20+38377G>T	NP_001313246.1:n.-20+38377G>T
NM_001326318.2:c.-20+38377G>T	NP_001313247.1:n.-20+38377G>T
NM_001326319.2:c.-20+17922G>T	NP_001313248.1:n.-20+17922G>T
NM_001326320.2:c.-20+38377G>T	NP_001313249.1:n.-20+38377G>T
NM_001326321.2:c.-20+38377G>T	NP_001313250.1:n.-20+38377G>T
NM_001326323.2:c.-20+38377G>T	NP_001313252.1:n.-20+38377G>T
NM_001326324.2:c.-20+38377G>T	NP_001313253.1:n.-20+38377G>T
NM_001326325.2:c.146+38377G>T	NP_001313254.1:n.146+38377G>T
NM_001326326.2:c.89+38377G>T	NP_001313255.1:n.89+38377G>T
NM_001326327.2:c.89+38377G>T	NP_001313256.1:n.89+38377G>T
NM_001326328.2:c.-20+38377G>T	NP_001313257.1:n.-20+38377G>T