Canonical Allele Identifier: CA399900040

Gene: CRHR1 LINC02210-CRHR1

Linked Data

• MyVariant Identifiers: chr17:g.43907819T>G (hg19) ; chr17:g.45830453T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45830453T>G , CM000679.2:g.45830453T>G	GRCh38
NC_000017.10:g.43907819T>G , CM000679.1:g.43907819T>G	GRCh37
NC_000017.9:g.41263600T>G	NCBI36
NG_009902.1:g.51192T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000580876.6:c.67T>G (CRHR1)	ENSP00000516345.1:p.Phe23Val
ENST00000580955.6:n.807T>G (CRHR1)
ENST00000705340.1:n.867T>G (CRHR1)
ENST00000705341.1:c.*269T>G (CRHR1)	ENSP00000516114.1:n.*269T>G
ENST00000705342.1:n.692T>G (CRHR1)
ENST00000705343.1:n.832T>G (CRHR1)
ENST00000705344.1:n.396T>G (CRHR1)
ENST00000314537.10:c.592T>G (CRHR1) MANE Select	ENSP00000326060.6:p.Phe198Val
ENST00000293493.11:c.679T>G (CRHR1)	ENSP00000293493.8:p.Phe227Val
ENST00000314537.9:c.592T>G (CRHR1)	ENSP00000326060.5:p.Phe198Val
ENST00000339069.9:c.289T>G (CRHR1)	ENSP00000340522.6:p.Phe97Val
ENST00000347197.9:c.*69T>G (CRHR1)	ENSP00000239167.7:n.*69T>G
ENST00000352855.9:c.472T>G (CRHR1)	ENSP00000344068.5:p.Phe158Val
ENST00000398285.7:c.679T>G (CRHR1)	ENSP00000381333.3:p.Phe227Val
ENST00000577353.5:c.592T>G (CRHR1)	ENSP00000462016.1:p.Phe198Val
ENST00000581479.1:n.54T>G (CRHR1)
ENST00000582766.5:n.650T>G (CRHR1)
ENST00000583888.1:c.339+239T>G (CRHR1)	ENSP00000462553.1:n.339+239T>G
ENST00000619154.4:c.386T>G (CRHR1)	ENSP00000484545.1:p.Leu129Arg
ENST00000634540.1:c.67T>G (LINC02210-CRHR1)	ENSP00000488912.1:p.Phe23Val
NM_001145146.1:c.679T>G (CRHR1)	NP_001138618.1:p.Phe227Val
NM_001145147.1:c.472T>G (CRHR1)	NP_001138619.1:p.Phe158Val
NM_001145148.1:c.592T>G (CRHR1)	NP_001138620.1:p.Phe198Val
NM_001256299.2:c.67T>G (LINC02210-CRHR1)	NP_001243228.1:p.Phe23Val
NM_001303016.1:c.289T>G (LINC02210-CRHR1)	NP_001289945.1:p.Phe97Val
NM_001303018.1:c.67T>G (CRHR1)	NP_001289947.1:p.Phe23Val
NM_001303020.1:c.289T>G (CRHR1)	NP_001289949.1:p.Phe97Val
NM_004382.4:c.592T>G (CRHR1)	NP_004373.2:p.Phe198Val
NM_001145146.2:c.679T>G (CRHR1)	NP_001138618.1:p.Phe227Val
NM_001145147.2:c.472T>G (CRHR1)	NP_001138619.1:p.Phe158Val
NM_001145148.2:c.592T>G (CRHR1)	NP_001138620.1:p.Phe198Val
NM_001256299.3:c.67T>G (LINC02210-CRHR1)	NP_001243228.1:p.Phe23Val
NM_001303018.2:c.67T>G (CRHR1)	NP_001289947.1:p.Phe23Val
NM_004382.5:c.592T>G (CRHR1) MANE Select	NP_004373.2:p.Phe198Val
NM_001303020.2:c.289T>G (CRHR1)	NP_001289949.1:p.Phe97Val