Canonical Allele Identifier: CA192896192

Gene: GRHPR

Linked Data

• COSMIC: COSN17154248
• MyVariant Identifiers: chr9:g.37436633_37436634insCT (hg19) ; chr9:g.37436636_37436637insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436636_37436637insCT , CM000671.2:g.37436636_37436637insCT	GRCh38
NC_000009.11:g.37436633_37436634insCT , CM000671.1:g.37436633_37436634insCT	GRCh37
NC_000009.10:g.37426633_37426634insCT	NCBI36
NG_008135.1:g.18927_18928insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-25_866-24insCT MANE Select	ENSP00000313432.6:n.866-25_866-24insCT
ENST00000318158.10:c.866-25_866-24insCT	ENSP00000313432.6:n.866-25_866-24insCT
ENST00000460882.5:n.893-25_893-24insCT
ENST00000480596.5:n.1567-25_1567-24insCT
ENST00000491488.5:n.571-25_571-24insCT
ENST00000494290.1:c.*52-245_*52-244insCT	ENSP00000432021.1:n.*52-245_*52-244insCT
ENST00000497693.1:n.4434-25_4434-24insCT
NM_012203.1:c.866-25_866-24insCT	NP_036335.1:n.866-25_866-24insCT
XM_005251631.1:c.545-25_545-24insCT	XP_005251688.1:n.545-25_545-24insCT
XM_011518073.1:c.464-25_464-24insCT	XP_011516375.1:n.464-25_464-24insCT
XM_017015320.2:c.946-775_946-774insCT	XP_016870809.1:n.946-775_946-774insCT
XM_017015321.2:c.866-775_866-774insCT	XP_016870810.1:n.866-775_866-774insCT
XM_017015323.2:c.544-775_544-774insCT	XP_016870812.1:n.544-775_544-774insCT
XM_024447716.1:c.1219-775_1219-774insCT	XP_024303484.1:n.1219-775_1219-774insCT
XM_024447717.1:c.1139-775_1139-774insCT	XP_024303485.1:n.1139-775_1139-774insCT
XR_002956828.1:n.1234-775_1234-774insCT
XR_002956829.1:n.1154-775_1154-774insCT
XR_002956830.1:n.2286-25_2286-24insCT
XR_002956831.1:n.1961-25_1961-24insCT
XR_002956832.1:n.1285-25_1285-24insCT
NM_012203.2:c.866-25_866-24insCT MANE Select	NP_036335.1:n.866-25_866-24insCT