Canonical Allele Identifier: CA1846868462

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428016_37428018delinsTGG , CM000671.2:g.37428016_37428018delinsTGG	GRCh38
NC_000009.11:g.37428013_37428015delinsTGG , CM000671.1:g.37428013_37428015delinsTGG	GRCh37
NC_000009.10:g.37418013_37418015delinsTGG	NCBI36
NG_008135.1:g.10307_10309delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-468_405-466delinsTGG MANE Select	ENSP00000313432.6:n.405-468_405-466delinsTGG
ENST00000318158.10:c.405-468_405-466delinsTGG	ENSP00000313432.6:n.405-468_405-466delinsTGG
ENST00000377824.8:n.442-468_442-466delinsTGG
ENST00000460882.5:n.432-468_432-466delinsTGG
ENST00000491488.5:n.110-468_110-466delinsTGG
ENST00000493368.5:n.462-468_462-466delinsTGG
ENST00000497693.1:n.311_313delinsTGG
ENST00000607784.1:c.405-468_405-466delinsTGG	ENSP00000475569.1:n.405-468_405-466delinsTGG
NM_012203.1:c.405-468_405-466delinsTGG	NP_036335.1:n.405-468_405-466delinsTGG
XM_005251631.1:c.84-468_84-466delinsTGG	XP_005251688.1:n.84-468_84-466delinsTGG
XM_011518073.1:c.-358-468_-358-466delinsTGG	XP_011516375.1:n.-358-468_-358-466delinsTGG
XR_929374.1:n.490-468_490-466delinsTGG
XM_017015320.2:c.405-468_405-466delinsTGG	XP_016870809.1:n.405-468_405-466delinsTGG
XM_017015321.2:c.405-468_405-466delinsTGG	XP_016870810.1:n.405-468_405-466delinsTGG
XM_017015323.2:c.-358-468_-358-466delinsTGG	XP_016870812.1:n.-358-468_-358-466delinsTGG
XM_024447716.1:c.678-468_678-466delinsTGG	XP_024303484.1:n.678-468_678-466delinsTGG
XM_024447717.1:c.678-468_678-466delinsTGG	XP_024303485.1:n.678-468_678-466delinsTGG
XR_002956828.1:n.693-468_693-466delinsTGG
XR_002956829.1:n.693-468_693-466delinsTGG
XR_002956830.1:n.464-468_464-466delinsTGG
XR_002956831.1:n.139-468_139-466delinsTGG
XR_002956832.1:n.464-468_464-466delinsTGG
NM_012203.2:c.405-468_405-466delinsTGG MANE Select	NP_036335.1:n.405-468_405-466delinsTGG