Canonical Allele Identifier: CA373443396

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429780A>C (hg19) ; chr9:g.37429783A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429783A>C , CM000671.2:g.37429783A>C	GRCh38
NC_000009.11:g.37429780A>C , CM000671.1:g.37429780A>C	GRCh37
NC_000009.10:g.37419780A>C	NCBI36
NG_008135.1:g.12074A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.545A>C MANE Select	ENSP00000313432.6:p.Tyr182Ser
ENST00000318158.10:c.545A>C	ENSP00000313432.6:p.Tyr182Ser
ENST00000377824.8:n.582A>C
ENST00000460882.5:n.572A>C
ENST00000480596.5:n.1246A>C
ENST00000491488.5:n.250A>C
ENST00000494290.1:c.116A>C	ENSP00000432021.1:p.Tyr39Ser
ENST00000497693.1:n.2078A>C
ENST00000607784.1:c.545A>C	ENSP00000475569.1:p.Tyr182Ser
NM_012203.1:c.545A>C	NP_036335.1:p.Tyr182Ser
XM_005251631.1:c.224A>C	XP_005251688.1:p.Tyr75Ser
XM_011518073.1:c.143A>C	XP_011516375.1:p.Tyr48Ser
XR_929374.1:n.990A>C
XM_017015320.2:c.545A>C	XP_016870809.1:p.Tyr182Ser
XM_017015321.2:c.545A>C	XP_016870810.1:p.Tyr182Ser
XM_017015323.2:c.143A>C	XP_016870812.1:p.Tyr48Ser
XM_024447716.1:c.818A>C	XP_024303484.1:p.Tyr273Ser
XM_024447717.1:c.818A>C	XP_024303485.1:p.Tyr273Ser
XR_002956828.1:n.833A>C
XR_002956829.1:n.833A>C
XR_002956830.1:n.604A>C
XR_002956831.1:n.279A>C
XR_002956832.1:n.964A>C
NM_012203.2:c.545A>C MANE Select	NP_036335.1:p.Tyr182Ser