Canonical Allele Identifier: CA373442762

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428522A>T (hg19) ; chr9:g.37428525A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428525A>T , CM000671.2:g.37428525A>T	GRCh38
NC_000009.11:g.37428522A>T , CM000671.1:g.37428522A>T	GRCh37
NC_000009.10:g.37418522A>T	NCBI36
NG_008135.1:g.10816A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.446A>T MANE Select	ENSP00000313432.6:p.Tyr149Phe
ENST00000318158.10:c.446A>T	ENSP00000313432.6:p.Tyr149Phe
ENST00000377824.8:n.483A>T
ENST00000460882.5:n.473A>T
ENST00000491488.5:n.151A>T
ENST00000493368.5:n.503A>T
ENST00000497693.1:n.820A>T
ENST00000607784.1:c.446A>T	ENSP00000475569.1:p.Tyr149Phe
NM_012203.1:c.446A>T	NP_036335.1:p.Tyr149Phe
XM_005251631.1:c.125A>T	XP_005251688.1:p.Tyr42Phe
XM_011518073.1:c.-317A>T	XP_011516375.1:n.-317A>T
XR_929374.1:n.531A>T
XM_017015320.2:c.446A>T	XP_016870809.1:p.Tyr149Phe
XM_017015321.2:c.446A>T	XP_016870810.1:p.Tyr149Phe
XM_017015323.2:c.-317A>T	XP_016870812.1:n.-317A>T
XM_024447716.1:c.719A>T	XP_024303484.1:p.Tyr240Phe
XM_024447717.1:c.719A>T	XP_024303485.1:p.Tyr240Phe
XR_002956828.1:n.734A>T
XR_002956829.1:n.734A>T
XR_002956830.1:n.505A>T
XR_002956831.1:n.180A>T
XR_002956832.1:n.505A>T
NM_012203.2:c.446A>T MANE Select	NP_036335.1:p.Tyr149Phe