Canonical Allele Identifier: CA465003995

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428547C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428550C>A , CM000671.2:g.37428550C>A	GRCh38
NC_000009.11:g.37428547C>A , CM000671.1:g.37428547C>A	GRCh37
NC_000009.10:g.37418547C>A	NCBI36
NG_008135.1:g.10841C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.471C>A MANE Select	ENSP00000313432.6:p.Gly157=
ENST00000318158.10:c.471C>A	ENSP00000313432.6:p.Gly157=
ENST00000377824.8:n.508C>A
ENST00000460882.5:n.498C>A
ENST00000480596.5:n.13C>A
ENST00000491488.5:n.176C>A
ENST00000493368.5:n.528C>A
ENST00000497693.1:n.845C>A
ENST00000607784.1:c.471C>A	ENSP00000475569.1:p.Gly157=
NM_012203.1:c.471C>A	NP_036335.1:p.Gly157=
XM_005251631.1:c.150C>A	XP_005251688.1:p.Gly50=
XM_011518073.1:c.-292C>A	XP_011516375.1:n.-292C>A
XR_929374.1:n.556C>A
XM_017015320.2:c.471C>A	XP_016870809.1:p.Gly157=
XM_017015321.2:c.471C>A	XP_016870810.1:p.Gly157=
XM_017015323.2:c.-292C>A	XP_016870812.1:n.-292C>A
XM_024447716.1:c.744C>A	XP_024303484.1:p.Gly248=
XM_024447717.1:c.744C>A	XP_024303485.1:p.Gly248=
XR_002956828.1:n.759C>A
XR_002956829.1:n.759C>A
XR_002956830.1:n.530C>A
XR_002956831.1:n.205C>A
XR_002956832.1:n.530C>A
NM_012203.2:c.471C>A MANE Select	NP_036335.1:p.Gly157=