Canonical Allele Identifier: CA373443400

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429781C>A (hg19) ; chr9:g.37429784C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429784C>A , CM000671.2:g.37429784C>A	GRCh38
NC_000009.11:g.37429781C>A , CM000671.1:g.37429781C>A	GRCh37
NC_000009.10:g.37419781C>A	NCBI36
NG_008135.1:g.12075C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.546C>A MANE Select	ENSP00000313432.6:p.Tyr182Ter
ENST00000318158.10:c.546C>A	ENSP00000313432.6:p.Tyr182Ter
ENST00000377824.8:n.583C>A
ENST00000460882.5:n.573C>A
ENST00000480596.5:n.1247C>A
ENST00000491488.5:n.251C>A
ENST00000494290.1:c.117C>A	ENSP00000432021.1:p.Tyr39Ter
ENST00000497693.1:n.2079C>A
ENST00000607784.1:c.546C>A	ENSP00000475569.1:p.Tyr182Ter
NM_012203.1:c.546C>A	NP_036335.1:p.Tyr182Ter
XM_005251631.1:c.225C>A	XP_005251688.1:p.Tyr75Ter
XM_011518073.1:c.144C>A	XP_011516375.1:p.Tyr48Ter
XR_929374.1:n.991C>A
XM_017015320.2:c.546C>A	XP_016870809.1:p.Tyr182Ter
XM_017015321.2:c.546C>A	XP_016870810.1:p.Tyr182Ter
XM_017015323.2:c.144C>A	XP_016870812.1:p.Tyr48Ter
XM_024447716.1:c.819C>A	XP_024303484.1:p.Tyr273Ter
XM_024447717.1:c.819C>A	XP_024303485.1:p.Tyr273Ter
XR_002956828.1:n.834C>A
XR_002956829.1:n.834C>A
XR_002956830.1:n.605C>A
XR_002956831.1:n.280C>A
XR_002956832.1:n.965C>A
NM_012203.2:c.546C>A MANE Select	NP_036335.1:p.Tyr182Ter