Canonical Allele Identifier: CA1846866365
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426549T= , CM000671.2:g.37426549T= GRCh38
NC_000009.11:g.37426546T= , CM000671.1:g.37426546T= GRCh37
NC_000009.10:g.37416546T= NCBI36
NG_008135.1:g.8840T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.299T= MANE Select ENSP00000313432.6:p.Val100=
ENST00000318158.10:c.299T= ENSP00000313432.6:p.Val100=
ENST00000377824.8:n.336T=
ENST00000460882.5:n.326T=
ENST00000487399.5:n.851T=
ENST00000491488.5:n.110-1935T=
ENST00000493368.5:n.356T=
ENST00000607784.1:c.299T= ENSP00000475569.1:p.Val100=
NM_012203.1:c.299T= NP_036335.1:p.Val100=
XM_005251631.1:c.84-1935T= XP_005251688.1:n.84-1935T=
XM_011518073.1:c.-464T= XP_011516375.1:n.-464T=
XR_929374.1:n.384T=
XM_017015320.2:c.299T= XP_016870809.1:p.Val100=
XM_017015321.2:c.299T= XP_016870810.1:p.Val100=
XM_017015323.2:c.-464T= XP_016870812.1:n.-464T=
XM_024447716.1:c.572T= XP_024303484.1:p.Val191=
XM_024447717.1:c.572T= XP_024303485.1:p.Val191=
XR_002956828.1:n.587T=
XR_002956829.1:n.587T=
XR_002956830.1:n.358T=
XR_002956831.1:n.139-1935T=
XR_002956832.1:n.358T=
NM_012203.2:c.299T= MANE Select NP_036335.1:p.Val100=