Canonical Allele Identifier: CA399900049

Gene: CRHR1 LINC02210-CRHR1

Linked Data

• dbSNP Id: rs2143236337
• MyVariant Identifiers: chr17:g.43907822C>G (hg19) ; chr17:g.45830456C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45830456C>G , CM000679.2:g.45830456C>G	GRCh38
NC_000017.10:g.43907822C>G , CM000679.1:g.43907822C>G	GRCh37
NC_000017.9:g.41263603C>G	NCBI36
NG_009902.1:g.51195C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000580876.6:c.70C>G (CRHR1)	ENSP00000516345.1:p.His24Asp
ENST00000580955.6:n.810C>G (CRHR1)
ENST00000705340.1:n.870C>G (CRHR1)
ENST00000705341.1:c.*272C>G (CRHR1)	ENSP00000516114.1:n.*272C>G
ENST00000705342.1:n.695C>G (CRHR1)
ENST00000705343.1:n.835C>G (CRHR1)
ENST00000705344.1:n.399C>G (CRHR1)
ENST00000314537.10:c.595C>G (CRHR1) MANE Select	ENSP00000326060.6:p.His199Asp
ENST00000293493.11:c.682C>G (CRHR1)	ENSP00000293493.8:p.His228Asp
ENST00000314537.9:c.595C>G (CRHR1)	ENSP00000326060.5:p.His199Asp
ENST00000339069.9:c.292C>G (CRHR1)	ENSP00000340522.6:p.His98Asp
ENST00000347197.9:c.*72C>G (CRHR1)	ENSP00000239167.7:n.*72C>G
ENST00000352855.9:c.475C>G (CRHR1)	ENSP00000344068.5:p.His159Asp
ENST00000398285.7:c.682C>G (CRHR1)	ENSP00000381333.3:p.His228Asp
ENST00000577353.5:c.595C>G (CRHR1)	ENSP00000462016.1:p.His199Asp
ENST00000581479.1:n.57C>G (CRHR1)
ENST00000582766.5:n.653C>G (CRHR1)
ENST00000583888.1:c.339+242C>G (CRHR1)	ENSP00000462553.1:n.339+242C>G
ENST00000619154.4:c.389C>G (CRHR1)	ENSP00000484545.1:p.Pro130Arg
ENST00000634540.1:c.70C>G (LINC02210-CRHR1)	ENSP00000488912.1:p.His24Asp
NM_001145146.1:c.682C>G (CRHR1)	NP_001138618.1:p.His228Asp
NM_001145147.1:c.475C>G (CRHR1)	NP_001138619.1:p.His159Asp
NM_001145148.1:c.595C>G (CRHR1)	NP_001138620.1:p.His199Asp
NM_001256299.2:c.70C>G (LINC02210-CRHR1)	NP_001243228.1:p.His24Asp
NM_001303016.1:c.292C>G (LINC02210-CRHR1)	NP_001289945.1:p.His98Asp
NM_001303018.1:c.70C>G (CRHR1)	NP_001289947.1:p.His24Asp
NM_001303020.1:c.292C>G (CRHR1)	NP_001289949.1:p.His98Asp
NM_004382.4:c.595C>G (CRHR1)	NP_004373.2:p.His199Asp
NM_001145146.2:c.682C>G (CRHR1)	NP_001138618.1:p.His228Asp
NM_001145147.2:c.475C>G (CRHR1)	NP_001138619.1:p.His159Asp
NM_001145148.2:c.595C>G (CRHR1)	NP_001138620.1:p.His199Asp
NM_001256299.3:c.70C>G (LINC02210-CRHR1)	NP_001243228.1:p.His24Asp
NM_001303018.2:c.70C>G (CRHR1)	NP_001289947.1:p.His24Asp
NM_004382.5:c.595C>G (CRHR1) MANE Select	NP_004373.2:p.His199Asp
NM_001303020.2:c.292C>G (CRHR1)	NP_001289949.1:p.His98Asp