Canonical Allele Identifier: CA8906367
Community Standard Title: NM_001142966.3(GREB1L):c.1062A>G (p.Ser354=)
Gene: GREB1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21440381A>G , CM000680.2:g.21440381A>G GRCh38
NC_000018.9:g.19020342A>G , CM000680.1:g.19020342A>G GRCh37
NC_000018.8:g.17274340A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001142966.3:c.1062A>G MANE Select NP_001136438.1:p.Ser354=
ENST00000424526.7:c.1062A>G MANE Select ENSP00000412060.1:p.Ser354=
NM_001142966.1:c.1062A>G NP_001136438.1:p.Ser354=
NM_001142966.2:c.1062A>G NP_001136438.1:p.Ser354=
ENST00000269218.10:c.1062A>G ENSP00000269218.6:p.Ser354=
ENST00000424526.5:c.1062A>G ENSP00000412060.1:p.Ser354=
ENST00000424526.6:c.1062A>G ENSP00000412060.1:p.Ser354=
ENST00000578368.5:n.1167A>G
ENST00000579454.1:c.583A>G
ENST00000579454.2:c.1191A>G ENSP00000463926.2:p.Ser397=
ENST00000580732.6:c.1062A>G ENSP00000464162.1:p.Ser354=
ENST00000584446.5:n.1333A>G
XM_006722547.1:c.1191A>G XP_006722610.1:p.Ser397=
XM_006722547.3:c.1191A>G XP_006722610.1:p.Ser397=
XM_011526176.1:c.1191A>G XP_011524478.1:p.Ser397=
XM_011526177.1:c.1191A>G XP_011524479.1:p.Ser397=
XM_011526178.1:c.1062A>G XP_011524480.1:p.Ser354=
XM_011526179.1:c.1191A>G XP_011524481.1:p.Ser397=
XM_011526179.3:c.1191A>G XP_011524481.1:p.Ser397=
XM_011526180.1:c.1191A>G XP_011524482.1:p.Ser397=
XM_011526181.1:c.1062A>G XP_011524483.1:p.Ser354=
XM_017025988.1:c.1191A>G XP_016881477.1:p.Ser397=
XM_017025989.1:c.1191A>G XP_016881478.1:p.Ser397=
XM_017025990.1:c.1191A>G XP_016881479.1:p.Ser397=
XM_017025991.1:c.1191A>G XP_016881480.1:p.Ser397=
XM_017025992.1:c.1062A>G XP_016881481.1:p.Ser354=
XM_017025993.1:c.1062A>G XP_016881482.1:p.Ser354=
XM_017025994.1:c.1191A>G XP_016881483.1:p.Ser397=
XM_017025995.1:c.1191A>G XP_016881484.1:p.Ser397=
XM_017025996.1:c.1062A>G XP_016881485.1:p.Ser354=
XR_001753366.1:n.134+10502T>C
XR_935269.1:n.172+10502T>C
XR_935270.1:n.172+10502T>C
XR_935271.1:n.172+10502T>C
XR_935272.1:n.172+10502T>C
XR_935272.2:n.141+10502T>C