Canonical Allele Identifier: CA2261940848

Gene: LINC02210 LINC02210-CRHR1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45641777A= , CM000679.2:g.45641777A=	GRCh38
NC_000017.10:g.43719143A= , CM000679.1:g.43719143A=	GRCh37
NC_000017.9:g.41074926A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001256299.2:c.-493+11619A= (LINC02210-CRHR1)	NP_001243228.1:n.-493+11619A=
NM_001256299.3:c.-493+11619A= (LINC02210-CRHR1)	NP_001243228.1:n.-493+11619A=
NM_001303016.1:c.-261+11619A= (LINC02210-CRHR1)	NP_001289945.1:n.-261+11619A=
NR_026906.2:n.613+1322A= (LINC02210)
NR_138257.1:n.3545A= (LINC02210)
NR_138258.1:n.434-4124A= (LINC02210)
NR_138259.1:n.2032+1322A= (LINC02210)
NR_138260.1:n.625-4124A= (LINC02210)
ENST00000578000.5:n.1935A= (LINC02210)
ENST00000580655.1:n.1416A= (LINC02210)
ENST00000585677.1:n.546+2257A= (LINC02210)
ENST00000586362.1:n.202-4124A= (LINC02210)
ENST00000587305.1:n.371+11619A= (LINC02210-CRHR1)
ENST00000591271.5:n.423-4124A= (LINC02210)
ENST00000592428.1:n.151+1322A= (LINC02210)
ENST00000634540.1:c.-493+11619A= (LINC02210-CRHR1)	ENSP00000488912.1:n.-493+11619A=