Canonical Allele Identifier: CA401734981

Gene: GREB1L

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21452220A>C , CM000680.2:g.21452220A>C	GRCh38
NC_000018.9:g.19032181A>C , CM000680.1:g.19032181A>C	GRCh37
NC_000018.8:g.17286179A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001142966.3:c.1984+3A>C MANE Select	NP_001136438.1:n.1984+3A>C
ENST00000424526.7:c.1984+3A>C MANE Select	ENSP00000412060.1:n.1984+3A>C
NM_001142966.1:c.1984+3A>C	NP_001136438.1:n.1984+3A>C
NM_001142966.2:c.1984+3A>C	NP_001136438.1:n.1984+3A>C
ENST00000269218.10:c.1657+3A>C	ENSP00000269218.6:n.1657+3A>C
ENST00000424526.5:c.1984+3A>C	ENSP00000412060.1:n.1984+3A>C
ENST00000424526.6:c.1984+3A>C	ENSP00000412060.1:n.1984+3A>C
ENST00000578368.5:n.2089+3A>C
ENST00000578955.1:n.188+3A>C
ENST00000579454.2:c.2113+3A>C	ENSP00000463926.2:n.2113+3A>C
ENST00000580732.6:c.1984+3A>C	ENSP00000464162.1:n.1984+3A>C
ENST00000581327.1:c.469A>C	ENSP00000463976.1:p.Asn157His
ENST00000584446.5:n.2255+3A>C
XM_006722547.1:c.2113+3A>C	XP_006722610.1:n.2113+3A>C
XM_006722547.3:c.2113+3A>C	XP_006722610.1:n.2113+3A>C
XM_011526176.1:c.2113+3A>C	XP_011524478.1:n.2113+3A>C
XM_011526177.1:c.2113+3A>C	XP_011524479.1:n.2113+3A>C
XM_011526178.1:c.1984+3A>C	XP_011524480.1:n.1984+3A>C
XM_011526179.1:c.2113+3A>C	XP_011524481.1:n.2113+3A>C
XM_011526179.3:c.2113+3A>C	XP_011524481.1:n.2113+3A>C
XM_011526180.1:c.1786+3A>C	XP_011524482.1:n.1786+3A>C
XM_011526181.1:c.1657+3A>C	XP_011524483.1:n.1657+3A>C
XM_017025988.1:c.2113+3A>C	XP_016881477.1:n.2113+3A>C
XM_017025989.1:c.2113+3A>C	XP_016881478.1:n.2113+3A>C
XM_017025990.1:c.2113+3A>C	XP_016881479.1:n.2113+3A>C
XM_017025991.1:c.2029+3A>C	XP_016881480.1:n.2029+3A>C
XM_017025992.1:c.1984+3A>C	XP_016881481.1:n.1984+3A>C
XM_017025993.1:c.1984+3A>C	XP_016881482.1:n.1984+3A>C
XM_017025994.1:c.1786+3A>C	XP_016881483.1:n.1786+3A>C
XM_017025995.1:c.1702+3A>C	XP_016881484.1:n.1702+3A>C
XM_017025996.1:c.1657+3A>C	XP_016881485.1:n.1657+3A>C