Canonical Allele Identifier: CA373441521

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37424909G>T (hg19) ; chr9:g.37424912G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424912G>T , CM000671.2:g.37424912G>T	GRCh38
NC_000009.11:g.37424909G>T , CM000671.1:g.37424909G>T	GRCh37
NC_000009.10:g.37414909G>T	NCBI36
NG_008135.1:g.7203G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.151G>T MANE Select	ENSP00000313432.6:p.Gly51Trp
ENST00000318158.10:c.151G>T	ENSP00000313432.6:p.Gly51Trp
ENST00000377824.8:n.188G>T
ENST00000460882.5:n.178G>T
ENST00000487399.5:n.160G>T
ENST00000491488.5:n.109+2079G>T
ENST00000493368.5:n.208G>T
ENST00000607784.1:c.151G>T	ENSP00000475569.1:p.Gly51Trp
NM_012203.1:c.151G>T	NP_036335.1:p.Gly51Trp
XM_005251631.1:c.83+2079G>T	XP_005251688.1:n.83+2079G>T
XM_011518073.1:c.-612G>T	XP_011516375.1:n.-612G>T
XR_929374.1:n.236G>T
XM_017015320.2:c.151G>T	XP_016870809.1:p.Gly51Trp
XM_017015321.2:c.151G>T	XP_016870810.1:p.Gly51Trp
XM_017015323.2:c.-612G>T	XP_016870812.1:n.-612G>T
XM_024447716.1:c.424G>T	XP_024303484.1:p.Gly142Trp
XM_024447717.1:c.424G>T	XP_024303485.1:p.Gly142Trp
XR_002956828.1:n.439G>T
XR_002956829.1:n.439G>T
XR_002956830.1:n.210G>T
XR_002956831.1:n.138+2079G>T
XR_002956832.1:n.210G>T
NM_012203.2:c.151G>T MANE Select	NP_036335.1:p.Gly51Trp