Canonical Allele Identifier: CA373443360

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429771G>T (hg19) ; chr9:g.37429774G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429774G>T , CM000671.2:g.37429774G>T	GRCh38
NC_000009.11:g.37429771G>T , CM000671.1:g.37429771G>T	GRCh37
NC_000009.10:g.37419771G>T	NCBI36
NG_008135.1:g.12065G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.536G>T MANE Select	ENSP00000313432.6:p.Arg179Ile
ENST00000318158.10:c.536G>T	ENSP00000313432.6:p.Arg179Ile
ENST00000377824.8:n.573G>T
ENST00000460882.5:n.563G>T
ENST00000480596.5:n.1237G>T
ENST00000491488.5:n.241G>T
ENST00000494290.1:c.107G>T	ENSP00000432021.1:p.Arg36Ile
ENST00000497693.1:n.2069G>T
ENST00000607784.1:c.536G>T	ENSP00000475569.1:p.Arg179Ile
NM_012203.1:c.536G>T	NP_036335.1:p.Arg179Ile
XM_005251631.1:c.215G>T	XP_005251688.1:p.Arg72Ile
XM_011518073.1:c.134G>T	XP_011516375.1:p.Arg45Ile
XR_929374.1:n.981G>T
XM_017015320.2:c.536G>T	XP_016870809.1:p.Arg179Ile
XM_017015321.2:c.536G>T	XP_016870810.1:p.Arg179Ile
XM_017015323.2:c.134G>T	XP_016870812.1:p.Arg45Ile
XM_024447716.1:c.809G>T	XP_024303484.1:p.Arg270Ile
XM_024447717.1:c.809G>T	XP_024303485.1:p.Arg270Ile
XR_002956828.1:n.824G>T
XR_002956829.1:n.824G>T
XR_002956830.1:n.595G>T
XR_002956831.1:n.270G>T
XR_002956832.1:n.955G>T
NM_012203.2:c.536G>T MANE Select	NP_036335.1:p.Arg179Ile