Canonical Allele Identifier: CA1846886829

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436898_37436900delinsAAG , CM000671.2:g.37436898_37436900delinsAAG	GRCh38
NC_000009.11:g.37436895_37436897delinsAAG , CM000671.1:g.37436895_37436897delinsAAG	GRCh37
NC_000009.10:g.37426895_37426897delinsAAG	NCBI36
NG_008135.1:g.19189_19191delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*116_*118delinsAAG MANE Select	ENSP00000313432.6:n.*116_*118delinsAAG
ENST00000318158.10:c.*116_*118delinsAAG	ENSP00000313432.6:n.*116_*118delinsAAG
ENST00000480596.5:n.1804_1806delinsAAG
ENST00000494290.1:c.*69_*71delinsAAG	ENSP00000432021.1:n.*69_*71delinsAAG
ENST00000497693.1:n.4671_4673delinsAAG
NM_012203.1:c.*116_*118delinsAAG	NP_036335.1:n.*116_*118delinsAAG
XM_005251631.1:c.*116_*118delinsAAG	XP_005251688.1:n.*116_*118delinsAAG
XM_011518073.1:c.*116_*118delinsAAG	XP_011516375.1:n.*116_*118delinsAAG
XM_017015320.2:c.946-513_946-511delinsAAG	XP_016870809.1:n.946-513_946-511delinsAAG
XM_017015321.2:c.866-513_866-511delinsAAG	XP_016870810.1:n.866-513_866-511delinsAAG
XM_017015323.2:c.544-513_544-511delinsAAG	XP_016870812.1:n.544-513_544-511delinsAAG
XM_024447716.1:c.1219-513_1219-511delinsAAG	XP_024303484.1:n.1219-513_1219-511delinsAAG
XM_024447717.1:c.1139-513_1139-511delinsAAG	XP_024303485.1:n.1139-513_1139-511delinsAAG
XR_002956828.1:n.1234-513_1234-511delinsAAG
XR_002956829.1:n.1154-513_1154-511delinsAAG
XR_002956830.1:n.2523_2525delinsAAG
XR_002956831.1:n.2198_2200delinsAAG
XR_002956832.1:n.1522_1524delinsAAG
NM_012203.2:c.*116_*118delinsAAG MANE Select	NP_036335.1:n.*116_*118delinsAAG