Canonical Allele Identifier: CA2842625531

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436840dup , CM000671.2:g.37436840dup	GRCh38
NC_000009.11:g.37436837dup , CM000671.1:g.37436837dup	GRCh37
NC_000009.10:g.37426837dup	NCBI36
NG_008135.1:g.19131dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*58dup MANE Select	ENSP00000313432.6:n.*58dup
ENST00000318158.10:c.*58dup	ENSP00000313432.6:n.*58dup
ENST00000460882.5:n.1072dup
ENST00000480596.5:n.1746dup
ENST00000494290.1:c.*52-41dup	ENSP00000432021.1:n.*52-41dup
ENST00000497693.1:n.4613dup
NM_012203.1:c.*58dup	NP_036335.1:n.*58dup
XM_005251631.1:c.*58dup	XP_005251688.1:n.*58dup
XM_011518073.1:c.*58dup	XP_011516375.1:n.*58dup
XM_017015320.2:c.946-571dup	XP_016870809.1:n.946-571dup
XM_017015321.2:c.866-571dup	XP_016870810.1:n.866-571dup
XM_017015323.2:c.544-571dup	XP_016870812.1:n.544-571dup
XM_024447716.1:c.1219-571dup	XP_024303484.1:n.1219-571dup
XM_024447717.1:c.1139-571dup	XP_024303485.1:n.1139-571dup
XR_002956828.1:n.1234-571dup
XR_002956829.1:n.1154-571dup
XR_002956830.1:n.2465dup
XR_002956831.1:n.2140dup
XR_002956832.1:n.1464dup
NM_012203.2:c.*58dup MANE Select	NP_036335.1:n.*58dup