Canonical Allele Identifier: CA373445453

Gene: GRHPR

Linked Data

• COSMIC: COSM363454
• MyVariant Identifiers: chr9:g.37436739G>T (hg19) ; chr9:g.37436742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436742G>T , CM000671.2:g.37436742G>T	GRCh38
NC_000009.11:g.37436739G>T , CM000671.1:g.37436739G>T	GRCh37
NC_000009.10:g.37426739G>T	NCBI36
NG_008135.1:g.19033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.947G>T MANE Select	ENSP00000313432.6:p.Gly316Val
ENST00000318158.10:c.947G>T	ENSP00000313432.6:p.Gly316Val
ENST00000460882.5:n.974G>T
ENST00000480596.5:n.1648G>T
ENST00000494290.1:c.*52-139G>T	ENSP00000432021.1:n.*52-139G>T
ENST00000497693.1:n.4515G>T
NM_012203.1:c.947G>T	NP_036335.1:p.Gly316Val
XM_005251631.1:c.626G>T	XP_005251688.1:p.Gly209Val
XM_011518073.1:c.545G>T	XP_011516375.1:p.Gly182Val
XM_017015320.2:c.946-669G>T	XP_016870809.1:n.946-669G>T
XM_017015321.2:c.866-669G>T	XP_016870810.1:n.866-669G>T
XM_017015323.2:c.544-669G>T	XP_016870812.1:n.544-669G>T
XM_024447716.1:c.1219-669G>T	XP_024303484.1:n.1219-669G>T
XM_024447717.1:c.1139-669G>T	XP_024303485.1:n.1139-669G>T
XR_002956828.1:n.1234-669G>T
XR_002956829.1:n.1154-669G>T
XR_002956830.1:n.2367G>T
XR_002956831.1:n.2042G>T
XR_002956832.1:n.1366G>T
NM_012203.2:c.947G>T MANE Select	NP_036335.1:p.Gly316Val