Canonical Allele Identifier: CA2262020629

Gene: CRHR1 LINC02210-CRHR1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45829303T= , CM000679.2:g.45829303T=	GRCh38
NC_000017.10:g.43906669T= , CM000679.1:g.43906669T=	GRCh37
NC_000017.9:g.41262450T=	NCBI36
NG_009902.1:g.50042T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580876.6:c.-110T= (CRHR1)	ENSP00000516345.1:n.-110T=
ENST00000580955.6:n.429T= (CRHR1)
ENST00000705340.1:n.691T= (CRHR1)
ENST00000705341.1:c.*93T= (CRHR1)	ENSP00000516114.1:n.*93T=
ENST00000705342.1:n.314T= (CRHR1)
ENST00000314537.10:c.416T= (CRHR1) MANE Select	ENSP00000326060.6:p.Val139=
ENST00000293493.11:c.416T= (CRHR1)	ENSP00000293493.8:p.Val139=
ENST00000314537.9:c.416T= (CRHR1)	ENSP00000326060.5:p.Val139=
ENST00000339069.9:c.113T= (CRHR1)	ENSP00000340522.6:p.Val38=
ENST00000347197.9:c.416T= (CRHR1)	ENSP00000239167.7:p.Val139=
ENST00000352855.9:c.296T= (CRHR1)	ENSP00000344068.5:p.Val99=
ENST00000398285.7:c.416T= (CRHR1)	ENSP00000381333.3:p.Val139=
ENST00000577353.5:c.416T= (CRHR1)	ENSP00000462016.1:p.Val139=
ENST00000580955.5:c.429T= (CRHR1)
ENST00000582766.5:n.272T= (CRHR1)
ENST00000583888.1:c.200T= (CRHR1)	ENSP00000462553.1:p.Val67=
ENST00000619154.4:c.210T= (CRHR1)	ENSP00000484545.1:p.Cys70=
ENST00000634540.1:c.-110T= (LINC02210-CRHR1)	ENSP00000488912.1:n.-110T=
NM_001145146.1:c.416T= (CRHR1)	NP_001138618.1:p.Val139=
NM_001145147.1:c.296T= (CRHR1)	NP_001138619.1:p.Val99=
NM_001145148.1:c.416T= (CRHR1)	NP_001138620.1:p.Val139=
NM_001256299.2:c.-110T= (LINC02210-CRHR1)	NP_001243228.1:n.-110T=
NM_001303016.1:c.113T= (LINC02210-CRHR1)	NP_001289945.1:p.Val38=
NM_001303018.1:c.-110T= (CRHR1)	NP_001289947.1:n.-110T=
NM_001303020.1:c.113T= (CRHR1)	NP_001289949.1:p.Val38=
NM_004382.4:c.416T= (CRHR1)	NP_004373.2:p.Val139=
NM_001145146.2:c.416T= (CRHR1)	NP_001138618.1:p.Val139=
NM_001145147.2:c.296T= (CRHR1)	NP_001138619.1:p.Val99=
NM_001145148.2:c.416T= (CRHR1)	NP_001138620.1:p.Val139=
NM_001256299.3:c.-110T= (LINC02210-CRHR1)	NP_001243228.1:n.-110T=
NM_001303018.2:c.-110T= (CRHR1)	NP_001289947.1:n.-110T=
NM_004382.5:c.416T= (CRHR1) MANE Select	NP_004373.2:p.Val139=
NM_001303020.2:c.113T= (CRHR1)	NP_001289949.1:p.Val38=