Canonical Allele Identifier: CA373444599
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37432131G>C , CM000671.2:g.37432131G>C GRCh38
NC_000009.11:g.37432128G>C , CM000671.1:g.37432128G>C GRCh37
NC_000009.10:g.37422128G>C NCBI36
NG_008135.1:g.14422G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.858G>C MANE Select ENSP00000313432.6:p.Lys286Asn
ENST00000318158.10:c.858G>C ENSP00000313432.6:p.Lys286Asn
ENST00000460882.5:n.885G>C
ENST00000480596.5:n.1559G>C
ENST00000482603.1:n.311G>C
ENST00000491488.5:n.563G>C
ENST00000494290.1:c.*51+980G>C ENSP00000432021.1:n.*51+980G>C
ENST00000497693.1:n.4426G>C
ENST00000512404.2:n.45G>C
ENST00000607784.1:c.858G>C ENSP00000475569.1:p.Lys286Asn
NM_012203.1:c.858G>C NP_036335.1:p.Lys286Asn
XM_005251631.1:c.537G>C XP_005251688.1:p.Lys179Asn
XM_011518073.1:c.456G>C XP_011516375.1:p.Lys152Asn
XM_017015320.2:c.858G>C XP_016870809.1:p.Lys286Asn
XM_017015321.2:c.858G>C XP_016870810.1:p.Lys286Asn
XM_017015323.2:c.456G>C XP_016870812.1:p.Lys152Asn
XM_024447716.1:c.1131G>C XP_024303484.1:p.Lys377Asn
XM_024447717.1:c.1131G>C XP_024303485.1:p.Lys377Asn
XR_002956828.1:n.1146G>C
XR_002956829.1:n.1146G>C
XR_002956830.1:n.2278G>C
XR_002956831.1:n.1953G>C
XR_002956832.1:n.1277G>C
NM_012203.2:c.858G>C MANE Select NP_036335.1:p.Lys286Asn