Canonical Allele Identifier: CA373443306

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429758-C-T
• MyVariant Identifiers: chr9:g.37429755C>T (hg19) ; chr9:g.37429758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429758C>T , CM000671.2:g.37429758C>T	GRCh38
NC_000009.11:g.37429755C>T , CM000671.1:g.37429755C>T	GRCh37
NC_000009.10:g.37419755C>T	NCBI36
NG_008135.1:g.12049C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.520C>T MANE Select	ENSP00000313432.6:p.Pro174Ser
ENST00000318158.10:c.520C>T	ENSP00000313432.6:p.Pro174Ser
ENST00000377824.8:n.557C>T
ENST00000460882.5:n.547C>T
ENST00000480596.5:n.1221C>T
ENST00000491488.5:n.225C>T
ENST00000494290.1:c.91C>T	ENSP00000432021.1:p.Pro31Ser
ENST00000497693.1:n.2053C>T
ENST00000607784.1:c.520C>T	ENSP00000475569.1:p.Pro174Ser
NM_012203.1:c.520C>T	NP_036335.1:p.Pro174Ser
XM_005251631.1:c.199C>T	XP_005251688.1:p.Pro67Ser
XM_011518073.1:c.118C>T	XP_011516375.1:p.Pro40Ser
XR_929374.1:n.965C>T
XM_017015320.2:c.520C>T	XP_016870809.1:p.Pro174Ser
XM_017015321.2:c.520C>T	XP_016870810.1:p.Pro174Ser
XM_017015323.2:c.118C>T	XP_016870812.1:p.Pro40Ser
XM_024447716.1:c.793C>T	XP_024303484.1:p.Pro265Ser
XM_024447717.1:c.793C>T	XP_024303485.1:p.Pro265Ser
XR_002956828.1:n.808C>T
XR_002956829.1:n.808C>T
XR_002956830.1:n.579C>T
XR_002956831.1:n.254C>T
XR_002956832.1:n.939C>T
NM_012203.2:c.520C>T MANE Select	NP_036335.1:p.Pro174Ser