Canonical Allele Identifier: CA465003865

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37426562T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426565T>C , CM000671.2:g.37426565T>C	GRCh38
NC_000009.11:g.37426562T>C , CM000671.1:g.37426562T>C	GRCh37
NC_000009.10:g.37416562T>C	NCBI36
NG_008135.1:g.8856T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.315T>C MANE Select	ENSP00000313432.6:p.Asp105=
ENST00000318158.10:c.315T>C	ENSP00000313432.6:p.Asp105=
ENST00000377824.8:n.352T>C
ENST00000460882.5:n.342T>C
ENST00000487399.5:n.867T>C
ENST00000491488.5:n.110-1919T>C
ENST00000493368.5:n.372T>C
ENST00000607784.1:c.315T>C	ENSP00000475569.1:p.Asp105=
NM_012203.1:c.315T>C	NP_036335.1:p.Asp105=
XM_005251631.1:c.84-1919T>C	XP_005251688.1:n.84-1919T>C
XM_011518073.1:c.-448T>C	XP_011516375.1:n.-448T>C
XR_929374.1:n.400T>C
XM_017015320.2:c.315T>C	XP_016870809.1:p.Asp105=
XM_017015321.2:c.315T>C	XP_016870810.1:p.Asp105=
XM_017015323.2:c.-448T>C	XP_016870812.1:n.-448T>C
XM_024447716.1:c.588T>C	XP_024303484.1:p.Asp196=
XM_024447717.1:c.588T>C	XP_024303485.1:p.Asp196=
XR_002956828.1:n.603T>C
XR_002956829.1:n.603T>C
XR_002956830.1:n.374T>C
XR_002956831.1:n.139-1919T>C
XR_002956832.1:n.374T>C
NM_012203.2:c.315T>C MANE Select	NP_036335.1:p.Asp105=