Canonical Allele Identifier: CA338006735

Gene: ARHGEF16

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3479540T>C , CM000663.2:g.3479540T>C	GRCh38
NC_000001.10:g.3396104T>C , CM000663.1:g.3396104T>C	GRCh37
NC_000001.9:g.3385964T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014448.4:c.1838T>C MANE Select	NP_055263.2:p.Val613Ala
ENST00000378378.9:c.1838T>C MANE Select	ENSP00000367629.4:p.Val613Ala
NM_014448.3:c.1838T>C	NP_055263.2:p.Val613Ala
ENST00000378371.6:c.974T>C	ENSP00000367622.2:p.Val325Ala
ENST00000378373.5:c.974T>C	ENSP00000367624.1:p.Val325Ala
ENST00000378378.8:c.1838T>C	ENSP00000367629.4:p.Val613Ala
ENST00000485984.1:n.1522T>C
XM_011541251.1:c.2003T>C	XP_011539553.1:p.Val668Ala
XM_011541252.1:c.2003T>C	XP_011539554.1:p.Val668Ala
XM_011541253.1:c.2003T>C	XP_011539555.1:p.Val668Ala
XM_017001049.1:c.1889T>C	XP_016856538.1:p.Val630Ala
XM_017001050.1:c.1838T>C	XP_016856539.1:p.Val613Ala
XM_017001051.1:c.1838T>C	XP_016856540.1:p.Val613Ala
XM_024446454.1:c.974T>C	XP_024302222.1:p.Val325Ala
XM_024446455.1:c.974T>C	XP_024302223.1:p.Val325Ala
XR_001737117.1:n.2769T>C
XR_946608.1:n.2086T>C