Canonical Allele Identifier: CA2770743664

Gene: DAAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39816467A>G , CM000668.2:g.39816467A>G	GRCh38
NC_000006.11:g.39784243A>G , CM000668.1:g.39784243A>G	GRCh37
NC_000006.10:g.39892221A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274867.9:c.-57+24002A>G MANE Select	ENSP00000274867.4:n.-57+24002A>G
ENST00000274867.8:c.-57+24002A>G	ENSP00000274867.4:n.-57+24002A>G
ENST00000398904.6:c.-57+23324A>G	ENSP00000381876.2:n.-57+23324A>G
ENST00000475489.5:n.70+24002A>G
ENST00000491083.2:n.90+24002A>G
ENST00000494405.2:c.-57+24002A>G	ENSP00000488196.1:n.-57+24002A>G
ENST00000538976.5:c.-57+23324A>G	ENSP00000437808.1:n.-57+23324A>G
ENST00000633794.1:c.-57+24002A>G	ENSP00000488831.1:n.-57+24002A>G
NM_001201427.1:c.-57+24002A>G	NP_001188356.1:n.-57+24002A>G
NM_015345.3:c.-57+23324A>G	NP_056160.2:n.-57+23324A>G
XM_006715043.1:c.-57+24002A>G	XP_006715106.1:n.-57+24002A>G
XM_006715046.2:c.-57+23324A>G	XP_006715109.1:n.-57+23324A>G
XR_926775.1:n.38+3230T>C
XM_006715043.2:c.-57+24002A>G	XP_006715106.1:n.-57+24002A>G
XM_006715046.4:c.-57+23324A>G	XP_006715109.1:n.-57+23324A>G
XM_017010630.1:c.13+21716A>G	XP_016866119.1:n.13+21716A>G
NM_001201427.2:c.-57+24002A>G MANE Select	NP_001188356.1:n.-57+24002A>G
NM_015345.4:c.-57+23324A>G	NP_056160.2:n.-57+23324A>G