Canonical Allele Identifier: CA373443319

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429759T>C (hg19) ; chr9:g.37429762T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429762T>C , CM000671.2:g.37429762T>C	GRCh38
NC_000009.11:g.37429759T>C , CM000671.1:g.37429759T>C	GRCh37
NC_000009.10:g.37419759T>C	NCBI36
NG_008135.1:g.12053T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.524T>C MANE Select	ENSP00000313432.6:p.Phe175Ser
ENST00000318158.10:c.524T>C	ENSP00000313432.6:p.Phe175Ser
ENST00000377824.8:n.561T>C
ENST00000460882.5:n.551T>C
ENST00000480596.5:n.1225T>C
ENST00000491488.5:n.229T>C
ENST00000494290.1:c.95T>C	ENSP00000432021.1:p.Phe32Ser
ENST00000497693.1:n.2057T>C
ENST00000607784.1:c.524T>C	ENSP00000475569.1:p.Phe175Ser
NM_012203.1:c.524T>C	NP_036335.1:p.Phe175Ser
XM_005251631.1:c.203T>C	XP_005251688.1:p.Phe68Ser
XM_011518073.1:c.122T>C	XP_011516375.1:p.Phe41Ser
XR_929374.1:n.969T>C
XM_017015320.2:c.524T>C	XP_016870809.1:p.Phe175Ser
XM_017015321.2:c.524T>C	XP_016870810.1:p.Phe175Ser
XM_017015323.2:c.122T>C	XP_016870812.1:p.Phe41Ser
XM_024447716.1:c.797T>C	XP_024303484.1:p.Phe266Ser
XM_024447717.1:c.797T>C	XP_024303485.1:p.Phe266Ser
XR_002956828.1:n.812T>C
XR_002956829.1:n.812T>C
XR_002956830.1:n.583T>C
XR_002956831.1:n.258T>C
XR_002956832.1:n.943T>C
NM_012203.2:c.524T>C MANE Select	NP_036335.1:p.Phe175Ser