Canonical Allele Identifier: CA913157697

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436725dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436728dup , CM000671.2:g.37436728dup	GRCh38
NC_000009.11:g.37436725dup , CM000671.1:g.37436725dup	GRCh37
NC_000009.10:g.37426725dup	NCBI36
NG_008135.1:g.19019dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.933dup MANE Select	ENSP00000313432.6:p.Asn312GlnfsTer13
ENST00000318158.10:c.933dup	ENSP00000313432.6:p.Asn312GlnfsTer13
ENST00000460882.5:n.960dup
ENST00000480596.5:n.1634dup
ENST00000494290.1:c.*52-153dup	ENSP00000432021.1:n.*52-153dup
ENST00000497693.1:n.4501dup
NM_012203.1:c.933dup	NP_036335.1:p.Asn312GlnfsTer13
XM_005251631.1:c.612dup	XP_005251688.1:p.Asn205GlnfsTer13
XM_011518073.1:c.531dup	XP_011516375.1:p.Asn178GlnfsTer13
XM_017015320.2:c.946-683dup	XP_016870809.1:n.946-683dup
XM_017015321.2:c.866-683dup	XP_016870810.1:n.866-683dup
XM_017015323.2:c.544-683dup	XP_016870812.1:n.544-683dup
XM_024447716.1:c.1219-683dup	XP_024303484.1:n.1219-683dup
XM_024447717.1:c.1139-683dup	XP_024303485.1:n.1139-683dup
XR_002956828.1:n.1234-683dup
XR_002956829.1:n.1154-683dup
XR_002956830.1:n.2353dup
XR_002956831.1:n.2028dup
XR_002956832.1:n.1352dup
NM_012203.2:c.933dup MANE Select	NP_036335.1:p.Asn312GlnfsTer13