Canonical Allele Identifier: CA863723377

Gene: GRHPR

Linked Data

• dbSNP Id: rs1423653387
• MyVariant Identifiers: chr9:g.37436752_37436753insC (hg19) ; chr9:g.37436755_37436756insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436757dup , CM000671.2:g.37436757dup	GRCh38
NC_000009.11:g.37436754dup , CM000671.1:g.37436754dup	GRCh37
NC_000009.10:g.37426754dup	NCBI36
NG_008135.1:g.19048dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.962dup MANE Select	ENSP00000313432.6:p.Met322AspfsTer3
ENST00000318158.10:c.962dup	ENSP00000313432.6:p.Met322AspfsTer3
ENST00000460882.5:n.989dup
ENST00000480596.5:n.1663dup
ENST00000494290.1:c.*52-124dup	ENSP00000432021.1:n.*52-124dup
ENST00000497693.1:n.4530dup
NM_012203.1:c.962dup	NP_036335.1:p.Met322AspfsTer3
XM_005251631.1:c.641dup	XP_005251688.1:p.Met215AspfsTer3
XM_011518073.1:c.560dup	XP_011516375.1:p.Met188AspfsTer3
XM_017015320.2:c.946-654dup	XP_016870809.1:n.946-654dup
XM_017015321.2:c.866-654dup	XP_016870810.1:n.866-654dup
XM_017015323.2:c.544-654dup	XP_016870812.1:n.544-654dup
XM_024447716.1:c.1219-654dup	XP_024303484.1:n.1219-654dup
XM_024447717.1:c.1139-654dup	XP_024303485.1:n.1139-654dup
XR_002956828.1:n.1234-654dup
XR_002956829.1:n.1154-654dup
XR_002956830.1:n.2382dup
XR_002956831.1:n.2057dup
XR_002956832.1:n.1381dup
NM_012203.2:c.962dup MANE Select	NP_036335.1:p.Met322AspfsTer3