Canonical Allele Identifier: CA465003783

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37424962G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424965G>T , CM000671.2:g.37424965G>T	GRCh38
NC_000009.11:g.37424962G>T , CM000671.1:g.37424962G>T	GRCh37
NC_000009.10:g.37414962G>T	NCBI36
NG_008135.1:g.7256G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.204G>T MANE Select	ENSP00000313432.6:p.Leu68=
ENST00000318158.10:c.204G>T	ENSP00000313432.6:p.Leu68=
ENST00000377824.8:n.241G>T
ENST00000460882.5:n.231G>T
ENST00000487399.5:n.213G>T
ENST00000491488.5:n.109+2132G>T
ENST00000493368.5:n.261G>T
ENST00000607784.1:c.204G>T	ENSP00000475569.1:p.Leu68=
NM_012203.1:c.204G>T	NP_036335.1:p.Leu68=
XM_005251631.1:c.83+2132G>T	XP_005251688.1:n.83+2132G>T
XM_011518073.1:c.-559G>T	XP_011516375.1:n.-559G>T
XR_929374.1:n.289G>T
XM_017015320.2:c.204G>T	XP_016870809.1:p.Leu68=
XM_017015321.2:c.204G>T	XP_016870810.1:p.Leu68=
XM_017015323.2:c.-559G>T	XP_016870812.1:n.-559G>T
XM_024447716.1:c.477G>T	XP_024303484.1:p.Leu159=
XM_024447717.1:c.477G>T	XP_024303485.1:p.Leu159=
XR_002956828.1:n.492G>T
XR_002956829.1:n.492G>T
XR_002956830.1:n.263G>T
XR_002956831.1:n.138+2132G>T
XR_002956832.1:n.263G>T
NM_012203.2:c.204G>T MANE Select	NP_036335.1:p.Leu68=