Canonical Allele Identifier: CA2579340560

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425862A>T , CM000671.2:g.37425862A>T	GRCh38
NC_000009.11:g.37425859A>T , CM000671.1:g.37425859A>T	GRCh37
NC_000009.10:g.37415859A>T	NCBI36
NG_008135.1:g.8153A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.215-60A>T MANE Select	ENSP00000313432.6:n.215-60A>T
ENST00000318158.10:c.215-60A>T	ENSP00000313432.6:n.215-60A>T
ENST00000377824.8:n.252-60A>T
ENST00000460882.5:n.242-60A>T
ENST00000487399.5:n.224-60A>T
ENST00000491488.5:n.110-2622A>T
ENST00000493368.5:n.272-60A>T
ENST00000607784.1:c.215-60A>T	ENSP00000475569.1:n.215-60A>T
NM_012203.1:c.215-60A>T	NP_036335.1:n.215-60A>T
XM_005251631.1:c.84-2622A>T	XP_005251688.1:n.84-2622A>T
XM_011518073.1:c.-548-60A>T	XP_011516375.1:n.-548-60A>T
XR_929374.1:n.300-60A>T
XM_017015320.2:c.215-60A>T	XP_016870809.1:n.215-60A>T
XM_017015321.2:c.215-60A>T	XP_016870810.1:n.215-60A>T
XM_017015323.2:c.-548-60A>T	XP_016870812.1:n.-548-60A>T
XM_024447716.1:c.488-60A>T	XP_024303484.1:n.488-60A>T
XM_024447717.1:c.488-60A>T	XP_024303485.1:n.488-60A>T
XR_002956828.1:n.503-60A>T
XR_002956829.1:n.503-60A>T
XR_002956830.1:n.274-60A>T
XR_002956831.1:n.139-2622A>T
XR_002956832.1:n.274-60A>T
NM_012203.2:c.215-60A>T MANE Select	NP_036335.1:n.215-60A>T