Canonical Allele Identifier: CA373442786

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428536A>T (hg19) ; chr9:g.37428539A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428539A>T , CM000671.2:g.37428539A>T	GRCh38
NC_000009.11:g.37428536A>T , CM000671.1:g.37428536A>T	GRCh37
NC_000009.10:g.37418536A>T	NCBI36
NG_008135.1:g.10830A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.460A>T MANE Select	ENSP00000313432.6:p.Ser154Cys
ENST00000318158.10:c.460A>T	ENSP00000313432.6:p.Ser154Cys
ENST00000377824.8:n.497A>T
ENST00000460882.5:n.487A>T
ENST00000480596.5:n.2A>T
ENST00000491488.5:n.165A>T
ENST00000493368.5:n.517A>T
ENST00000497693.1:n.834A>T
ENST00000607784.1:c.460A>T	ENSP00000475569.1:p.Ser154Cys
NM_012203.1:c.460A>T	NP_036335.1:p.Ser154Cys
XM_005251631.1:c.139A>T	XP_005251688.1:p.Ser47Cys
XM_011518073.1:c.-303A>T	XP_011516375.1:n.-303A>T
XR_929374.1:n.545A>T
XM_017015320.2:c.460A>T	XP_016870809.1:p.Ser154Cys
XM_017015321.2:c.460A>T	XP_016870810.1:p.Ser154Cys
XM_017015323.2:c.-303A>T	XP_016870812.1:n.-303A>T
XM_024447716.1:c.733A>T	XP_024303484.1:p.Ser245Cys
XM_024447717.1:c.733A>T	XP_024303485.1:p.Ser245Cys
XR_002956828.1:n.748A>T
XR_002956829.1:n.748A>T
XR_002956830.1:n.519A>T
XR_002956831.1:n.194A>T
XR_002956832.1:n.519A>T
NM_012203.2:c.460A>T MANE Select	NP_036335.1:p.Ser154Cys