Canonical Allele Identifier: CA12191558

Gene: DAAM2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39832238A>G , CM000668.2:g.39832238A>G	GRCh38
NC_000006.11:g.39800014A>G , CM000668.1:g.39800014A>G	GRCh37
NC_000006.10:g.39907992A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274867.9:c.-56-24009A>G MANE Select	ENSP00000274867.4:n.-56-24009A>G
ENST00000274867.8:c.-56-24009A>G	ENSP00000274867.4:n.-56-24009A>G
ENST00000398904.6:c.-56-24009A>G	ENSP00000381876.2:n.-56-24009A>G
ENST00000475489.5:n.71-24009A>G
ENST00000491083.2:n.91-24009A>G
ENST00000494405.2:c.-56-24009A>G	ENSP00000488196.1:n.-56-24009A>G
ENST00000538976.5:c.-56-24009A>G	ENSP00000437808.1:n.-56-24009A>G
ENST00000633794.1:c.-56-24009A>G	ENSP00000488831.1:n.-56-24009A>G
NM_001201427.1:c.-56-24009A>G	NP_001188356.1:n.-56-24009A>G
NM_015345.3:c.-56-24009A>G	NP_056160.2:n.-56-24009A>G
XM_006715039.2:c.85+10014A>G	XP_006715102.2:n.85+10014A>G
XM_006715040.2:c.85+10014A>G	XP_006715103.2:n.85+10014A>G
XM_006715042.1:c.-57+10765A>G	XP_006715105.1:n.-57+10765A>G
XM_006715043.1:c.-56-24009A>G	XP_006715106.1:n.-56-24009A>G
XM_006715045.2:c.-57+1869A>G	XP_006715108.1:n.-57+1869A>G
XM_006715046.2:c.-56-24009A>G	XP_006715109.1:n.-56-24009A>G
XM_011514447.1:c.13+12061A>G	XP_011512749.1:n.13+12061A>G
XM_006715039.3:c.241+10014A>G	XP_006715102.3:n.241+10014A>G
XM_006715040.3:c.241+10014A>G	XP_006715103.3:n.241+10014A>G
XM_006715042.2:c.-57+10765A>G	XP_006715105.1:n.-57+10765A>G
XM_006715043.2:c.-56-24009A>G	XP_006715106.1:n.-56-24009A>G
XM_006715045.3:c.-57+1869A>G	XP_006715108.1:n.-57+1869A>G
XM_006715046.4:c.-56-24009A>G	XP_006715109.1:n.-56-24009A>G
XM_017010630.1:c.14-24009A>G	XP_016866119.1:n.14-24009A>G
NM_001201427.2:c.-56-24009A>G MANE Select	NP_001188356.1:n.-56-24009A>G
NM_015345.4:c.-56-24009A>G	NP_056160.2:n.-56-24009A>G