Canonical Allele Identifier: CA399899995
Gene: CRHR1 HGNC NCBI
LINC02210-CRHR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45830436C>T , CM000679.2:g.45830436C>T GRCh38
NC_000017.10:g.43907802C>T , CM000679.1:g.43907802C>T GRCh37
NC_000017.9:g.41263583C>T NCBI36
NG_009902.1:g.51175C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000580876.6:c.50C>T (CRHR1) ENSP00000516345.1:p.Thr17Ile
ENST00000580955.6:n.790C>T (CRHR1)
ENST00000705340.1:n.850C>T (CRHR1)
ENST00000705341.1:c.*252C>T (CRHR1) ENSP00000516114.1:n.*252C>T
ENST00000705342.1:n.675C>T (CRHR1)
ENST00000705343.1:n.815C>T (CRHR1)
ENST00000705344.1:n.379C>T (CRHR1)
ENST00000314537.10:c.575C>T (CRHR1) MANE Select ENSP00000326060.6:p.Thr192Ile
ENST00000293493.11:c.662C>T (CRHR1) ENSP00000293493.8:p.Thr221Ile
ENST00000314537.9:c.575C>T (CRHR1) ENSP00000326060.5:p.Thr192Ile
ENST00000339069.9:c.272C>T (CRHR1) ENSP00000340522.6:p.Thr91Ile
ENST00000347197.9:c.*52C>T (CRHR1) ENSP00000239167.7:n.*52C>T
ENST00000352855.9:c.455C>T (CRHR1) ENSP00000344068.5:p.Thr152Ile
ENST00000398285.7:c.662C>T (CRHR1) ENSP00000381333.3:p.Thr221Ile
ENST00000577353.5:c.575C>T (CRHR1) ENSP00000462016.1:p.Thr192Ile
ENST00000581479.1:n.37C>T (CRHR1)
ENST00000582766.5:n.633C>T (CRHR1)
ENST00000583888.1:c.339+222C>T (CRHR1) ENSP00000462553.1:n.339+222C>T
ENST00000619154.4:c.369C>T (CRHR1) ENSP00000484545.1:p.Asp123=
ENST00000634540.1:c.50C>T (LINC02210-CRHR1) ENSP00000488912.1:p.Thr17Ile
NM_001145146.1:c.662C>T (CRHR1) NP_001138618.1:p.Thr221Ile
NM_001145147.1:c.455C>T (CRHR1) NP_001138619.1:p.Thr152Ile
NM_001145148.1:c.575C>T (CRHR1) NP_001138620.1:p.Thr192Ile
NM_001256299.2:c.50C>T (LINC02210-CRHR1) NP_001243228.1:p.Thr17Ile
NM_001303016.1:c.272C>T (LINC02210-CRHR1) NP_001289945.1:p.Thr91Ile
NM_001303018.1:c.50C>T (CRHR1) NP_001289947.1:p.Thr17Ile
NM_001303020.1:c.272C>T (CRHR1) NP_001289949.1:p.Thr91Ile
NM_004382.4:c.575C>T (CRHR1) NP_004373.2:p.Thr192Ile
NM_001145146.2:c.662C>T (CRHR1) NP_001138618.1:p.Thr221Ile
NM_001145147.2:c.455C>T (CRHR1) NP_001138619.1:p.Thr152Ile
NM_001145148.2:c.575C>T (CRHR1) NP_001138620.1:p.Thr192Ile
NM_001256299.3:c.50C>T (LINC02210-CRHR1) NP_001243228.1:p.Thr17Ile
NM_001303018.2:c.50C>T (CRHR1) NP_001289947.1:p.Thr17Ile
NM_004382.5:c.575C>T (CRHR1) MANE Select NP_004373.2:p.Thr192Ile
NM_001303020.2:c.272C>T (CRHR1) NP_001289949.1:p.Thr91Ile