Canonical Allele Identifier: CA6674138

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66392379G>A , CM000674.2:g.66392379G>A	GRCh38
NC_000012.11:g.66786159G>A , CM000674.1:g.66786159G>A	GRCh37
NC_000012.10:g.65072426G>A	NCBI36
NG_021400.1:g.291767C>T
NG_021400.2:g.681887C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001366722.1:c.2393C>T MANE Select	NP_001353651.1:p.Thr798Met
ENST00000359742.9:c.2393C>T MANE Select	ENSP00000352780.4:p.Thr798Met
NM_001178074.1:c.2237C>T	NP_001171545.1:p.Thr746Met
NM_001178074.2:c.2237C>T	NP_001171545.1:p.Thr746Met
NM_001366723.1:c.2312C>T	NP_001353652.1:p.Thr771Met
NM_001366724.1:c.2315C>T	NP_001353653.1:p.Thr772Met
NM_001379345.1:c.2471C>T	NP_001366274.1:p.Thr824Met
NM_001379346.1:c.2393C>T	NP_001366275.1:p.Thr798Met
NM_001379347.1:c.2315C>T	NP_001366276.1:p.Thr772Met
NM_001379348.1:c.2312C>T	NP_001366277.1:p.Thr771Met
NM_001379349.1:c.2240C>T	NP_001366278.1:p.Thr747Met
NM_001379351.1:c.2237C>T	NP_001366280.1:p.Thr746Met
NM_021150.3:c.2237C>T	NP_066973.2:p.Thr746Met
NM_021150.4:c.2237C>T	NP_066973.2:p.Thr746Met
ENST00000359742.8:c.2393C>T	ENSP00000352780.4:p.Thr798Met
ENST00000398016.7:c.2237C>T	ENSP00000381098.3:p.Thr746Met
ENST00000536215.5:c.1913C>T	ENSP00000446011.1:p.Thr638Met
ENST00000538164.5:c.1837C>T
ENST00000538211.5:c.2237C>T	ENSP00000446047.1:p.Thr746Met
ENST00000540433.5:c.2069C>T	ENSP00000446024.1:p.Thr690Met
ENST00000540854.5:c.338-43133C>T	ENSP00000443006.1:n.338-43133C>T
ENST00000541299.1:n.154C>T
ENST00000696989.1:c.2462C>T	ENSP00000513025.1:p.Thr821Met
XM_005268754.3:c.2396C>T	XP_005268811.1:p.Thr799Met
XM_005268754.4:c.2396C>T	XP_005268811.1:p.Thr799Met
XM_005268757.3:c.2315C>T	XP_005268814.1:p.Thr772Met
XM_005268757.4:c.2315C>T	XP_005268814.1:p.Thr772Met
XM_011538089.1:c.2618C>T	XP_011536391.1:p.Thr873Met
XM_011538090.1:c.2618C>T	XP_011536392.1:p.Thr873Met
XM_011538091.1:c.2462C>T	XP_011536393.1:p.Thr821Met
XM_011538092.1:c.2462C>T	XP_011536394.1:p.Thr821Met
XM_011538093.1:c.2393C>T	XP_011536395.1:p.Thr798Met
XM_011538094.1:c.2225C>T	XP_011536396.1:p.Thr742Met
XM_017019098.1:c.2618C>T	XP_016874587.1:p.Thr873Met
XM_017019099.1:c.2471C>T	XP_016874588.1:p.Thr824Met
XM_017019100.1:c.2462C>T	XP_016874589.1:p.Thr821Met