Canonical Allele Identifier: CA399900294

Gene: CRHR1 LINC02210-CRHR1

Linked Data

• gnomAD v4: 17-45830550-T-C
• MyVariant Identifiers: chr17:g.43907916T>C (hg19) ; chr17:g.45830550T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45830550T>C , CM000679.2:g.45830550T>C	GRCh38
NC_000017.10:g.43907916T>C , CM000679.1:g.43907916T>C	GRCh37
NC_000017.9:g.41263697T>C	NCBI36
NG_009902.1:g.51289T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580876.6:c.164T>C (CRHR1)	ENSP00000516345.1:p.Met55Thr
ENST00000580955.6:n.904T>C (CRHR1)
ENST00000705340.1:n.964T>C (CRHR1)
ENST00000705341.1:c.*366T>C (CRHR1)	ENSP00000516114.1:n.*366T>C
ENST00000705342.1:n.789T>C (CRHR1)
ENST00000705343.1:n.929T>C (CRHR1)
ENST00000705344.1:n.493T>C (CRHR1)
ENST00000314537.10:c.689T>C (CRHR1) MANE Select	ENSP00000326060.6:p.Met230Thr
ENST00000293493.11:c.776T>C (CRHR1)	ENSP00000293493.8:p.Met259Thr
ENST00000314537.9:c.689T>C (CRHR1)	ENSP00000326060.5:p.Met230Thr
ENST00000339069.9:c.386T>C (CRHR1)	ENSP00000340522.6:p.Met129Thr
ENST00000347197.9:c.*166T>C (CRHR1)	ENSP00000239167.7:n.*166T>C
ENST00000352855.9:c.569T>C (CRHR1)	ENSP00000344068.5:p.Met190Thr
ENST00000398285.7:c.776T>C (CRHR1)	ENSP00000381333.3:p.Met259Thr
ENST00000577353.5:c.689T>C (CRHR1)	ENSP00000462016.1:p.Met230Thr
ENST00000581479.1:n.151T>C (CRHR1)
ENST00000582766.5:n.747T>C (CRHR1)
ENST00000583888.1:c.340-330T>C (CRHR1)	ENSP00000462553.1:n.340-330T>C
ENST00000619154.4:c.*18T>C (CRHR1)	ENSP00000484545.1:n.*18T>C
ENST00000634540.1:c.164T>C (LINC02210-CRHR1)	ENSP00000488912.1:p.Met55Thr
NM_001145146.1:c.776T>C (CRHR1)	NP_001138618.1:p.Met259Thr
NM_001145147.1:c.569T>C (CRHR1)	NP_001138619.1:p.Met190Thr
NM_001145148.1:c.689T>C (CRHR1)	NP_001138620.1:p.Met230Thr
NM_001256299.2:c.164T>C (LINC02210-CRHR1)	NP_001243228.1:p.Met55Thr
NM_001303016.1:c.386T>C (LINC02210-CRHR1)	NP_001289945.1:p.Met129Thr
NM_001303018.1:c.164T>C (CRHR1)	NP_001289947.1:p.Met55Thr
NM_001303020.1:c.386T>C (CRHR1)	NP_001289949.1:p.Met129Thr
NM_004382.4:c.689T>C (CRHR1)	NP_004373.2:p.Met230Thr
NM_001145146.2:c.776T>C (CRHR1)	NP_001138618.1:p.Met259Thr
NM_001145147.2:c.569T>C (CRHR1)	NP_001138619.1:p.Met190Thr
NM_001145148.2:c.689T>C (CRHR1)	NP_001138620.1:p.Met230Thr
NM_001256299.3:c.164T>C (LINC02210-CRHR1)	NP_001243228.1:p.Met55Thr
NM_001303018.2:c.164T>C (CRHR1)	NP_001289947.1:p.Met55Thr
NM_004382.5:c.689T>C (CRHR1) MANE Select	NP_004373.2:p.Met230Thr
NM_001303020.2:c.386T>C (CRHR1)	NP_001289949.1:p.Met129Thr