Canonical Allele Identifier: CA373445447

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436736C>T (hg19) ; chr9:g.37436739C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436739C>T , CM000671.2:g.37436739C>T	GRCh38
NC_000009.11:g.37436736C>T , CM000671.1:g.37436736C>T	GRCh37
NC_000009.10:g.37426736C>T	NCBI36
NG_008135.1:g.19030C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.944C>T MANE Select	ENSP00000313432.6:p.Ala315Val
ENST00000318158.10:c.944C>T	ENSP00000313432.6:p.Ala315Val
ENST00000460882.5:n.971C>T
ENST00000480596.5:n.1645C>T
ENST00000494290.1:c.*52-142C>T	ENSP00000432021.1:n.*52-142C>T
ENST00000497693.1:n.4512C>T
NM_012203.1:c.944C>T	NP_036335.1:p.Ala315Val
XM_005251631.1:c.623C>T	XP_005251688.1:p.Ala208Val
XM_011518073.1:c.542C>T	XP_011516375.1:p.Ala181Val
XM_017015320.2:c.946-672C>T	XP_016870809.1:n.946-672C>T
XM_017015321.2:c.866-672C>T	XP_016870810.1:n.866-672C>T
XM_017015323.2:c.544-672C>T	XP_016870812.1:n.544-672C>T
XM_024447716.1:c.1219-672C>T	XP_024303484.1:n.1219-672C>T
XM_024447717.1:c.1139-672C>T	XP_024303485.1:n.1139-672C>T
XR_002956828.1:n.1234-672C>T
XR_002956829.1:n.1154-672C>T
XR_002956830.1:n.2364C>T
XR_002956831.1:n.2039C>T
XR_002956832.1:n.1363C>T
NM_012203.2:c.944C>T MANE Select	NP_036335.1:p.Ala315Val