Canonical Allele Identifier: CA373445339

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436684A>T (hg19) ; chr9:g.37436687A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436687A>T , CM000671.2:g.37436687A>T	GRCh38
NC_000009.11:g.37436684A>T , CM000671.1:g.37436684A>T	GRCh37
NC_000009.10:g.37426684A>T	NCBI36
NG_008135.1:g.18978A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.892A>T MANE Select	ENSP00000313432.6:p.Thr298Ser
ENST00000318158.10:c.892A>T	ENSP00000313432.6:p.Thr298Ser
ENST00000460882.5:n.919A>T
ENST00000480596.5:n.1593A>T
ENST00000491488.5:n.597A>T
ENST00000494290.1:c.*52-194A>T	ENSP00000432021.1:n.*52-194A>T
ENST00000497693.1:n.4460A>T
NM_012203.1:c.892A>T	NP_036335.1:p.Thr298Ser
XM_005251631.1:c.571A>T	XP_005251688.1:p.Thr191Ser
XM_011518073.1:c.490A>T	XP_011516375.1:p.Thr164Ser
XM_017015320.2:c.946-724A>T	XP_016870809.1:n.946-724A>T
XM_017015321.2:c.866-724A>T	XP_016870810.1:n.866-724A>T
XM_017015323.2:c.544-724A>T	XP_016870812.1:n.544-724A>T
XM_024447716.1:c.1219-724A>T	XP_024303484.1:n.1219-724A>T
XM_024447717.1:c.1139-724A>T	XP_024303485.1:n.1139-724A>T
XR_002956828.1:n.1234-724A>T
XR_002956829.1:n.1154-724A>T
XR_002956830.1:n.2312A>T
XR_002956831.1:n.1987A>T
XR_002956832.1:n.1311A>T
NM_012203.2:c.892A>T MANE Select	NP_036335.1:p.Thr298Ser