Canonical Allele Identifier: CA465003942

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428481T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428484T>C , CM000671.2:g.37428484T>C	GRCh38
NC_000009.11:g.37428481T>C , CM000671.1:g.37428481T>C	GRCh37
NC_000009.10:g.37418481T>C	NCBI36
NG_008135.1:g.10775T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405T>C MANE Select	ENSP00000313432.6:p.Asn135=
ENST00000318158.10:c.405T>C	ENSP00000313432.6:p.Asn135=
ENST00000377824.8:n.442T>C
ENST00000460882.5:n.432T>C
ENST00000491488.5:n.110T>C
ENST00000493368.5:n.462T>C
ENST00000497693.1:n.779T>C
ENST00000607784.1:c.405T>C	ENSP00000475569.1:p.Asn135=
NM_012203.1:c.405T>C	NP_036335.1:p.Asn135=
XM_005251631.1:c.84T>C	XP_005251688.1:p.Asp28=
XM_011518073.1:c.-358T>C	XP_011516375.1:n.-358T>C
XR_929374.1:n.490T>C
XM_017015320.2:c.405T>C	XP_016870809.1:p.Asn135=
XM_017015321.2:c.405T>C	XP_016870810.1:p.Asn135=
XM_017015323.2:c.-358T>C	XP_016870812.1:n.-358T>C
XM_024447716.1:c.678T>C	XP_024303484.1:p.Asn226=
XM_024447717.1:c.678T>C	XP_024303485.1:p.Asn226=
XR_002956828.1:n.693T>C
XR_002956829.1:n.693T>C
XR_002956830.1:n.464T>C
XR_002956831.1:n.139T>C
XR_002956832.1:n.464T>C
NM_012203.2:c.405T>C MANE Select	NP_036335.1:p.Asn135=