Canonical Allele Identifier: CA863722923

Gene: GRHPR

Linked Data

• dbSNP Id: rs1554749576
• MyVariant Identifiers: chr9:g.37436469_37436470insA (hg19) ; chr9:g.37436472_37436473insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436472_37436473insA , CM000671.2:g.37436472_37436473insA	GRCh38
NC_000009.11:g.37436469_37436470insA , CM000671.1:g.37436469_37436470insA	GRCh37
NC_000009.10:g.37426469_37426470insA	NCBI36
NG_008135.1:g.18763_18764insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-189_866-188insA MANE Select	ENSP00000313432.6:n.866-189_866-188insA
ENST00000318158.10:c.866-189_866-188insA	ENSP00000313432.6:n.866-189_866-188insA
ENST00000460882.5:n.893-189_893-188insA
ENST00000480596.5:n.1567-189_1567-188insA
ENST00000491488.5:n.571-189_571-188insA
ENST00000494290.1:c.*52-409_*52-408insA	ENSP00000432021.1:n.*52-409_*52-408insA
ENST00000497693.1:n.4434-189_4434-188insA
NM_012203.1:c.866-189_866-188insA	NP_036335.1:n.866-189_866-188insA
XM_005251631.1:c.545-189_545-188insA	XP_005251688.1:n.545-189_545-188insA
XM_011518073.1:c.464-189_464-188insA	XP_011516375.1:n.464-189_464-188insA
XM_017015320.2:c.946-939_946-938insA	XP_016870809.1:n.946-939_946-938insA
XM_017015321.2:c.866-939_866-938insA	XP_016870810.1:n.866-939_866-938insA
XM_017015323.2:c.544-939_544-938insA	XP_016870812.1:n.544-939_544-938insA
XM_024447716.1:c.1219-939_1219-938insA	XP_024303484.1:n.1219-939_1219-938insA
XM_024447717.1:c.1139-939_1139-938insA	XP_024303485.1:n.1139-939_1139-938insA
XR_002956828.1:n.1234-939_1234-938insA
XR_002956829.1:n.1154-939_1154-938insA
XR_002956830.1:n.2286-189_2286-188insA
XR_002956831.1:n.1961-189_1961-188insA
XR_002956832.1:n.1285-189_1285-188insA
NM_012203.2:c.866-189_866-188insA MANE Select	NP_036335.1:n.866-189_866-188insA