Canonical Allele Identifier: CA373442760

Gene: GRHPR

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.446A>C MANE Select	ENSP00000313432.6:p.Tyr149Ser
ENST00000318158.10:c.446A>C	ENSP00000313432.6:p.Tyr149Ser
ENST00000377824.8:n.483A>C
ENST00000460882.5:n.473A>C
ENST00000491488.5:n.151A>C
ENST00000493368.5:n.503A>C
ENST00000497693.1:n.820A>C
ENST00000607784.1:c.446A>C	ENSP00000475569.1:p.Tyr149Ser
NM_012203.1:c.446A>C	NP_036335.1:p.Tyr149Ser
XM_005251631.1:c.125A>C	XP_005251688.1:p.Tyr42Ser
XM_011518073.1:c.-317A>C	XP_011516375.1:n.-317A>C
XR_929374.1:n.531A>C
XM_017015320.2:c.446A>C	XP_016870809.1:p.Tyr149Ser
XM_017015321.2:c.446A>C	XP_016870810.1:p.Tyr149Ser
XM_017015323.2:c.-317A>C	XP_016870812.1:n.-317A>C
XM_024447716.1:c.719A>C	XP_024303484.1:p.Tyr240Ser
XM_024447717.1:c.719A>C	XP_024303485.1:p.Tyr240Ser
XR_002956828.1:n.734A>C
XR_002956829.1:n.734A>C
XR_002956830.1:n.505A>C
XR_002956831.1:n.180A>C
XR_002956832.1:n.505A>C
NM_012203.2:c.446A>C MANE Select	NP_036335.1:p.Tyr149Ser