Canonical Allele Identifier: CA1224492843

Gene: ENAH

Linked Data

• dbSNP Id: rs2096210616

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225488890A>C , CM000663.2:g.225488890A>C	GRCh38
NC_000001.10:g.225676592A>C , CM000663.1:g.225676592A>C	GRCh37
NC_000001.9:g.223743215A>C	NCBI36
NG_051578.1:g.176156T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696609.1:c.*8885T>G	ENSP00000512753.1:n.*8885T>G
ENST00000366843.7:c.*8885T>G MANE Select	ENSP00000355808.2:n.*8885T>G
ENST00000366844.7:c.*8885T>G	ENSP00000355809.2:n.*8885T>G
NM_001008493.1:c.*8885T>G	NP_001008493.1:n.*8885T>G
NM_018212.4:c.*8885T>G	NP_060682.2:n.*8885T>G
NM_001008493.2:c.*8885T>G	NP_001008493.1:n.*8885T>G
NM_018212.5:c.*8885T>G	NP_060682.2:n.*8885T>G
XM_017001751.1:c.*8885T>G	XP_016857240.1:n.*8885T>G
XM_024448309.1:c.*8885T>G	XP_024304077.1:n.*8885T>G
XM_024448310.1:c.*8885T>G	XP_024304078.1:n.*8885T>G
XM_024448311.1:c.*8885T>G	XP_024304079.1:n.*8885T>G
XM_024448313.1:c.*8885T>G	XP_024304081.1:n.*8885T>G
XM_024448314.1:c.*8885T>G	XP_024304082.1:n.*8885T>G
XM_024448315.1:c.*8885T>G	XP_024304083.1:n.*8885T>G
XM_024448316.1:c.*8885T>G	XP_024304084.1:n.*8885T>G
XM_024448317.1:c.*8885T>G	XP_024304085.1:n.*8885T>G
NM_001008493.3:c.*8885T>G	NP_001008493.1:n.*8885T>G
NM_001377481.1:c.*8885T>G	NP_001364410.1:n.*8885T>G
NM_001377482.1:c.*8885T>G	NP_001364411.1:n.*8885T>G
NM_001377483.1:c.*8885T>G	NP_001364412.1:n.*8885T>G
NM_018212.6:c.*8885T>G MANE Select	NP_060682.2:n.*8885T>G