Canonical Allele Identifier: CA465004437

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37432134T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432137T>C , CM000671.2:g.37432137T>C	GRCh38
NC_000009.11:g.37432134T>C , CM000671.1:g.37432134T>C	GRCh37
NC_000009.10:g.37422134T>C	NCBI36
NG_008135.1:g.14428T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.864T>C MANE Select	ENSP00000313432.6:p.Cys288=
ENST00000318158.10:c.864T>C	ENSP00000313432.6:p.Cys288=
ENST00000460882.5:n.891T>C
ENST00000480596.5:n.1565T>C
ENST00000482603.1:n.317T>C
ENST00000491488.5:n.569T>C
ENST00000494290.1:c.*51+986T>C	ENSP00000432021.1:n.*51+986T>C
ENST00000497693.1:n.4432T>C
ENST00000512404.2:n.51T>C
ENST00000607784.1:c.864T>C	ENSP00000475569.1:p.Cys288=
NM_012203.1:c.864T>C	NP_036335.1:p.Cys288=
XM_005251631.1:c.543T>C	XP_005251688.1:p.Cys181=
XM_011518073.1:c.462T>C	XP_011516375.1:p.Cys154=
XM_017015320.2:c.864T>C	XP_016870809.1:p.Cys288=
XM_017015321.2:c.864T>C	XP_016870810.1:p.Cys288=
XM_017015323.2:c.462T>C	XP_016870812.1:p.Cys154=
XM_024447716.1:c.1137T>C	XP_024303484.1:p.Cys379=
XM_024447717.1:c.1137T>C	XP_024303485.1:p.Cys379=
XR_002956828.1:n.1152T>C
XR_002956829.1:n.1152T>C
XR_002956830.1:n.2284T>C
XR_002956831.1:n.1959T>C
XR_002956832.1:n.1283T>C
NM_012203.2:c.864T>C MANE Select	NP_036335.1:p.Cys288=