Canonical Allele Identifier: CA465006842

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436719A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436722A>T , CM000671.2:g.37436722A>T	GRCh38
NC_000009.11:g.37436719A>T , CM000671.1:g.37436719A>T	GRCh37
NC_000009.10:g.37426719A>T	NCBI36
NG_008135.1:g.19013A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.927A>T MANE Select	ENSP00000313432.6:p.Ala309=
ENST00000318158.10:c.927A>T	ENSP00000313432.6:p.Ala309=
ENST00000460882.5:n.954A>T
ENST00000480596.5:n.1628A>T
ENST00000494290.1:c.*52-159A>T	ENSP00000432021.1:n.*52-159A>T
ENST00000497693.1:n.4495A>T
NM_012203.1:c.927A>T	NP_036335.1:p.Ala309=
XM_005251631.1:c.606A>T	XP_005251688.1:p.Ala202=
XM_011518073.1:c.525A>T	XP_011516375.1:p.Ala175=
XM_017015320.2:c.946-689A>T	XP_016870809.1:n.946-689A>T
XM_017015321.2:c.866-689A>T	XP_016870810.1:n.866-689A>T
XM_017015323.2:c.544-689A>T	XP_016870812.1:n.544-689A>T
XM_024447716.1:c.1219-689A>T	XP_024303484.1:n.1219-689A>T
XM_024447717.1:c.1139-689A>T	XP_024303485.1:n.1139-689A>T
XR_002956828.1:n.1234-689A>T
XR_002956829.1:n.1154-689A>T
XR_002956830.1:n.2347A>T
XR_002956831.1:n.2022A>T
XR_002956832.1:n.1346A>T
NM_012203.2:c.927A>T MANE Select	NP_036335.1:p.Ala309=