Canonical Allele Identifier: CA399900024

Gene: CRHR1 LINC02210-CRHR1

Linked Data

• MyVariant Identifiers: chr17:g.43907813A>T (hg19) ; chr17:g.45830447A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45830447A>T , CM000679.2:g.45830447A>T	GRCh38
NC_000017.10:g.43907813A>T , CM000679.1:g.43907813A>T	GRCh37
NC_000017.9:g.41263594A>T	NCBI36
NG_009902.1:g.51186A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000580876.6:c.61A>T (CRHR1)	ENSP00000516345.1:p.Asn21Tyr
ENST00000580955.6:n.801A>T (CRHR1)
ENST00000705340.1:n.861A>T (CRHR1)
ENST00000705341.1:c.*263A>T (CRHR1)	ENSP00000516114.1:n.*263A>T
ENST00000705342.1:n.686A>T (CRHR1)
ENST00000705343.1:n.826A>T (CRHR1)
ENST00000705344.1:n.390A>T (CRHR1)
ENST00000314537.10:c.586A>T (CRHR1) MANE Select	ENSP00000326060.6:p.Asn196Tyr
ENST00000293493.11:c.673A>T (CRHR1)	ENSP00000293493.8:p.Asn225Tyr
ENST00000314537.9:c.586A>T (CRHR1)	ENSP00000326060.5:p.Asn196Tyr
ENST00000339069.9:c.283A>T (CRHR1)	ENSP00000340522.6:p.Asn95Tyr
ENST00000347197.9:c.*63A>T (CRHR1)	ENSP00000239167.7:n.*63A>T
ENST00000352855.9:c.466A>T (CRHR1)	ENSP00000344068.5:p.Asn156Tyr
ENST00000398285.7:c.673A>T (CRHR1)	ENSP00000381333.3:p.Asn225Tyr
ENST00000577353.5:c.586A>T (CRHR1)	ENSP00000462016.1:p.Asn196Tyr
ENST00000581479.1:n.48A>T (CRHR1)
ENST00000582766.5:n.644A>T (CRHR1)
ENST00000583888.1:c.339+233A>T (CRHR1)	ENSP00000462553.1:n.339+233A>T
ENST00000619154.4:c.380A>T (CRHR1)	ENSP00000484545.1:p.Gln127Leu
ENST00000634540.1:c.61A>T (LINC02210-CRHR1)	ENSP00000488912.1:p.Asn21Tyr
NM_001145146.1:c.673A>T (CRHR1)	NP_001138618.1:p.Asn225Tyr
NM_001145147.1:c.466A>T (CRHR1)	NP_001138619.1:p.Asn156Tyr
NM_001145148.1:c.586A>T (CRHR1)	NP_001138620.1:p.Asn196Tyr
NM_001256299.2:c.61A>T (LINC02210-CRHR1)	NP_001243228.1:p.Asn21Tyr
NM_001303016.1:c.283A>T (LINC02210-CRHR1)	NP_001289945.1:p.Asn95Tyr
NM_001303018.1:c.61A>T (CRHR1)	NP_001289947.1:p.Asn21Tyr
NM_001303020.1:c.283A>T (CRHR1)	NP_001289949.1:p.Asn95Tyr
NM_004382.4:c.586A>T (CRHR1)	NP_004373.2:p.Asn196Tyr
NM_001145146.2:c.673A>T (CRHR1)	NP_001138618.1:p.Asn225Tyr
NM_001145147.2:c.466A>T (CRHR1)	NP_001138619.1:p.Asn156Tyr
NM_001145148.2:c.586A>T (CRHR1)	NP_001138620.1:p.Asn196Tyr
NM_001256299.3:c.61A>T (LINC02210-CRHR1)	NP_001243228.1:p.Asn21Tyr
NM_001303018.2:c.61A>T (CRHR1)	NP_001289947.1:p.Asn21Tyr
NM_004382.5:c.586A>T (CRHR1) MANE Select	NP_004373.2:p.Asn196Tyr
NM_001303020.2:c.283A>T (CRHR1)	NP_001289949.1:p.Asn95Tyr