Canonical Allele Identifier: CA373441733

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37424966G>T (hg19) ; chr9:g.37424969G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424969G>T , CM000671.2:g.37424969G>T	GRCh38
NC_000009.11:g.37424966G>T , CM000671.1:g.37424966G>T	GRCh37
NC_000009.10:g.37414966G>T	NCBI36
NG_008135.1:g.7260G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.208G>T MANE Select	ENSP00000313432.6:p.Ala70Ser
ENST00000318158.10:c.208G>T	ENSP00000313432.6:p.Ala70Ser
ENST00000377824.8:n.245G>T
ENST00000460882.5:n.235G>T
ENST00000487399.5:n.217G>T
ENST00000491488.5:n.109+2136G>T
ENST00000493368.5:n.265G>T
ENST00000607784.1:c.208G>T	ENSP00000475569.1:p.Ala70Ser
NM_012203.1:c.208G>T	NP_036335.1:p.Ala70Ser
XM_005251631.1:c.83+2136G>T	XP_005251688.1:n.83+2136G>T
XM_011518073.1:c.-555G>T	XP_011516375.1:n.-555G>T
XR_929374.1:n.293G>T
XM_017015320.2:c.208G>T	XP_016870809.1:p.Ala70Ser
XM_017015321.2:c.208G>T	XP_016870810.1:p.Ala70Ser
XM_017015323.2:c.-555G>T	XP_016870812.1:n.-555G>T
XM_024447716.1:c.481G>T	XP_024303484.1:p.Ala161Ser
XM_024447717.1:c.481G>T	XP_024303485.1:p.Ala161Ser
XR_002956828.1:n.496G>T
XR_002956829.1:n.496G>T
XR_002956830.1:n.267G>T
XR_002956831.1:n.138+2136G>T
XR_002956832.1:n.267G>T
NM_012203.2:c.208G>T MANE Select	NP_036335.1:p.Ala70Ser