Canonical Allele Identifier: CA500359392
Gene: CRHR1 HGNC NCBI
LINC02210-CRHR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.43907920C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45830554C>T , CM000679.2:g.45830554C>T GRCh38
NC_000017.10:g.43907920C>T , CM000679.1:g.43907920C>T GRCh37
NC_000017.9:g.41263701C>T NCBI36
NG_009902.1:g.51293C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580876.6:c.168C>T (CRHR1) ENSP00000516345.1:p.Phe56=
ENST00000580955.6:n.908C>T (CRHR1)
ENST00000705340.1:n.968C>T (CRHR1)
ENST00000705341.1:c.*370C>T (CRHR1) ENSP00000516114.1:n.*370C>T
ENST00000705342.1:n.793C>T (CRHR1)
ENST00000705343.1:n.933C>T (CRHR1)
ENST00000705344.1:n.497C>T (CRHR1)
ENST00000314537.10:c.693C>T (CRHR1) MANE Select ENSP00000326060.6:p.Phe231=
ENST00000293493.11:c.780C>T (CRHR1) ENSP00000293493.8:p.Phe260=
ENST00000314537.9:c.693C>T (CRHR1) ENSP00000326060.5:p.Phe231=
ENST00000339069.9:c.390C>T (CRHR1) ENSP00000340522.6:p.Phe130=
ENST00000347197.9:c.*170C>T (CRHR1) ENSP00000239167.7:n.*170C>T
ENST00000352855.9:c.573C>T (CRHR1) ENSP00000344068.5:p.Phe191=
ENST00000398285.7:c.780C>T (CRHR1) ENSP00000381333.3:p.Phe260=
ENST00000577353.5:c.693C>T (CRHR1) ENSP00000462016.1:p.Phe231=
ENST00000581479.1:n.155C>T (CRHR1)
ENST00000582766.5:n.751C>T (CRHR1)
ENST00000583888.1:c.340-326C>T (CRHR1) ENSP00000462553.1:n.340-326C>T
ENST00000619154.4:c.*22C>T (CRHR1) ENSP00000484545.1:n.*22C>T
ENST00000634540.1:c.168C>T (LINC02210-CRHR1) ENSP00000488912.1:p.Phe56=
NM_001145146.1:c.780C>T (CRHR1) NP_001138618.1:p.Phe260=
NM_001145147.1:c.573C>T (CRHR1) NP_001138619.1:p.Phe191=
NM_001145148.1:c.693C>T (CRHR1) NP_001138620.1:p.Phe231=
NM_001256299.2:c.168C>T (LINC02210-CRHR1) NP_001243228.1:p.Phe56=
NM_001303016.1:c.390C>T (LINC02210-CRHR1) NP_001289945.1:p.Phe130=
NM_001303018.1:c.168C>T (CRHR1) NP_001289947.1:p.Phe56=
NM_001303020.1:c.390C>T (CRHR1) NP_001289949.1:p.Phe130=
NM_004382.4:c.693C>T (CRHR1) NP_004373.2:p.Phe231=
NM_001145146.2:c.780C>T (CRHR1) NP_001138618.1:p.Phe260=
NM_001145147.2:c.573C>T (CRHR1) NP_001138619.1:p.Phe191=
NM_001145148.2:c.693C>T (CRHR1) NP_001138620.1:p.Phe231=
NM_001256299.3:c.168C>T (LINC02210-CRHR1) NP_001243228.1:p.Phe56=
NM_001303018.2:c.168C>T (CRHR1) NP_001289947.1:p.Phe56=
NM_004382.5:c.693C>T (CRHR1) MANE Select NP_004373.2:p.Phe231=
NM_001303020.2:c.390C>T (CRHR1) NP_001289949.1:p.Phe130=