Canonical Allele Identifier: CA2770743663

Gene: DAAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39816455G>C , CM000668.2:g.39816455G>C	GRCh38
NC_000006.11:g.39784231G>C , CM000668.1:g.39784231G>C	GRCh37
NC_000006.10:g.39892209G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274867.9:c.-57+23990G>C MANE Select	ENSP00000274867.4:n.-57+23990G>C
ENST00000274867.8:c.-57+23990G>C	ENSP00000274867.4:n.-57+23990G>C
ENST00000398904.6:c.-57+23312G>C	ENSP00000381876.2:n.-57+23312G>C
ENST00000475489.5:n.70+23990G>C
ENST00000491083.2:n.90+23990G>C
ENST00000494405.2:c.-57+23990G>C	ENSP00000488196.1:n.-57+23990G>C
ENST00000538976.5:c.-57+23312G>C	ENSP00000437808.1:n.-57+23312G>C
ENST00000633794.1:c.-57+23990G>C	ENSP00000488831.1:n.-57+23990G>C
NM_001201427.1:c.-57+23990G>C	NP_001188356.1:n.-57+23990G>C
NM_015345.3:c.-57+23312G>C	NP_056160.2:n.-57+23312G>C
XM_006715043.1:c.-57+23990G>C	XP_006715106.1:n.-57+23990G>C
XM_006715046.2:c.-57+23312G>C	XP_006715109.1:n.-57+23312G>C
XR_926775.1:n.38+3242C>G
XM_006715043.2:c.-57+23990G>C	XP_006715106.1:n.-57+23990G>C
XM_006715046.4:c.-57+23312G>C	XP_006715109.1:n.-57+23312G>C
XM_017010630.1:c.13+21704G>C	XP_016866119.1:n.13+21704G>C
NM_001201427.2:c.-57+23990G>C MANE Select	NP_001188356.1:n.-57+23990G>C
NM_015345.4:c.-57+23312G>C	NP_056160.2:n.-57+23312G>C