Canonical Allele Identifier: CA2579340791

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436616G>A , CM000671.2:g.37436616G>A	GRCh38
NC_000009.11:g.37436613G>A , CM000671.1:g.37436613G>A	GRCh37
NC_000009.10:g.37426613G>A	NCBI36
NG_008135.1:g.18907G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.866-45G>A MANE Select	ENSP00000313432.6:n.866-45G>A
ENST00000318158.10:c.866-45G>A	ENSP00000313432.6:n.866-45G>A
ENST00000460882.5:n.893-45G>A
ENST00000480596.5:n.1567-45G>A
ENST00000491488.5:n.571-45G>A
ENST00000494290.1:c.*52-265G>A	ENSP00000432021.1:n.*52-265G>A
ENST00000497693.1:n.4434-45G>A
NM_012203.1:c.866-45G>A	NP_036335.1:n.866-45G>A
XM_005251631.1:c.545-45G>A	XP_005251688.1:n.545-45G>A
XM_011518073.1:c.464-45G>A	XP_011516375.1:n.464-45G>A
XM_017015320.2:c.946-795G>A	XP_016870809.1:n.946-795G>A
XM_017015321.2:c.866-795G>A	XP_016870810.1:n.866-795G>A
XM_017015323.2:c.544-795G>A	XP_016870812.1:n.544-795G>A
XM_024447716.1:c.1219-795G>A	XP_024303484.1:n.1219-795G>A
XM_024447717.1:c.1139-795G>A	XP_024303485.1:n.1139-795G>A
XR_002956828.1:n.1234-795G>A
XR_002956829.1:n.1154-795G>A
XR_002956830.1:n.2286-45G>A
XR_002956831.1:n.1961-45G>A
XR_002956832.1:n.1285-45G>A
NM_012203.2:c.866-45G>A MANE Select	NP_036335.1:n.866-45G>A