Canonical Allele Identifier: CA863723516

Gene: GRHPR

Linked Data

• dbSNP Id: rs1242037620
• MyVariant Identifiers: chr9:g.37436907_37436908insAT (hg19) ; chr9:g.37436910_37436911insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436915_37436916dup , CM000671.2:g.37436915_37436916dup	GRCh38
NC_000009.11:g.37436912_37436913dup , CM000671.1:g.37436912_37436913dup	GRCh37
NC_000009.10:g.37426912_37426913dup	NCBI36
NG_008135.1:g.19206_19207dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*133_*134dup MANE Select	ENSP00000313432.6:n.*133_*134dup
ENST00000318158.10:c.*133_*134dup	ENSP00000313432.6:n.*133_*134dup
ENST00000480596.5:n.1821_1822dup
ENST00000494290.1:c.*86_*87dup	ENSP00000432021.1:n.*86_*87dup
ENST00000497693.1:n.4688_4689dup
NM_012203.1:c.*133_*134dup	NP_036335.1:n.*133_*134dup
XM_005251631.1:c.*133_*134dup	XP_005251688.1:n.*133_*134dup
XM_011518073.1:c.*133_*134dup	XP_011516375.1:n.*133_*134dup
XM_017015320.2:c.946-496_946-495dup	XP_016870809.1:n.946-496_946-495dup
XM_017015321.2:c.866-496_866-495dup	XP_016870810.1:n.866-496_866-495dup
XM_017015323.2:c.544-496_544-495dup	XP_016870812.1:n.544-496_544-495dup
XM_024447716.1:c.1219-496_1219-495dup	XP_024303484.1:n.1219-496_1219-495dup
XM_024447717.1:c.1139-496_1139-495dup	XP_024303485.1:n.1139-496_1139-495dup
XR_002956828.1:n.1234-496_1234-495dup
XR_002956829.1:n.1154-496_1154-495dup
XR_002956830.1:n.2540_2541dup
XR_002956831.1:n.2215_2216dup
XR_002956832.1:n.1539_1540dup
NM_012203.2:c.*133_*134dup MANE Select	NP_036335.1:n.*133_*134dup