Canonical Allele Identifier: CA10791734

Gene: ENAH

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225515783A>G , CM000663.2:g.225515783A>G	GRCh38
NC_000001.10:g.225703485A>G , CM000663.1:g.225703485A>G	GRCh37
NC_000001.9:g.223770108A>G	NCBI36
NG_051578.1:g.149263T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696609.1:c.1232-883T>C	ENSP00000512753.1:n.1232-883T>C
ENST00000366843.7:c.914-883T>C MANE Select	ENSP00000355808.2:n.914-883T>C
ENST00000366843.6:c.914-883T>C	ENSP00000355808.2:n.914-883T>C
ENST00000366844.7:c.914-883T>C	ENSP00000355809.2:n.914-883T>C
ENST00000635051.1:c.1610-883T>C	ENSP00000489607.1:n.1610-883T>C
NM_001008493.1:c.914-883T>C	NP_001008493.1:n.914-883T>C
NM_018212.4:c.914-883T>C	NP_060682.2:n.914-883T>C
XM_005273187.1:c.956-883T>C	XP_005273244.1:n.956-883T>C
XM_006711795.1:c.1013-883T>C	XP_006711858.1:n.1013-883T>C
XM_006711796.1:c.1013-883T>C	XP_006711859.1:n.1013-883T>C
XM_006711797.1:c.902-883T>C	XP_006711860.1:n.902-883T>C
XM_011544229.1:c.932-883T>C	XP_011542531.1:n.932-883T>C
XM_011544230.1:c.971-883T>C	XP_011542532.1:n.971-883T>C
XM_011544231.1:c.932-883T>C	XP_011542533.1:n.932-883T>C
XM_011544232.1:c.956-883T>C	XP_011542534.1:n.956-883T>C
XM_011544233.1:c.875-883T>C	XP_011542535.1:n.875-883T>C
XM_011544234.1:c.845-883T>C	XP_011542536.1:n.845-883T>C
XM_011544235.1:c.548-883T>C	XP_011542537.1:n.548-883T>C
NM_001008493.2:c.914-883T>C	NP_001008493.1:n.914-883T>C
NM_018212.5:c.914-883T>C	NP_060682.2:n.914-883T>C
XM_011544229.2:c.1757-883T>C	XP_011542531.2:n.1757-883T>C
XM_017001746.2:c.1769-883T>C	XP_016857235.1:n.1769-883T>C
XM_017001747.1:c.1769-883T>C	XP_016857236.1:n.1769-883T>C
XM_017001748.1:c.1700-883T>C	XP_016857237.1:n.1700-883T>C
XM_017001749.1:c.1757-883T>C	XP_016857238.1:n.1757-883T>C
XM_017001750.1:c.1658-883T>C	XP_016857239.1:n.1658-883T>C
XM_017001751.1:c.1700-883T>C	XP_016857240.1:n.1700-883T>C
XM_017001752.1:c.1589-883T>C	XP_016857241.1:n.1589-883T>C
XM_024448305.1:c.2453-883T>C	XP_024304073.1:n.2453-883T>C
XM_024448306.1:c.2441-883T>C	XP_024304074.1:n.2441-883T>C
XM_024448307.1:c.2453-883T>C	XP_024304075.1:n.2453-883T>C
XM_024448308.1:c.2384-883T>C	XP_024304076.1:n.2384-883T>C
XM_024448309.1:c.1709-883T>C	XP_024304077.1:n.1709-883T>C
XM_024448310.1:c.1709-883T>C	XP_024304078.1:n.1709-883T>C
XM_024448311.1:c.1667-883T>C	XP_024304079.1:n.1667-883T>C
XM_024448313.1:c.1640-883T>C	XP_024304081.1:n.1640-883T>C
XM_024448314.1:c.1628-883T>C	XP_024304082.1:n.1628-883T>C
XM_024448315.1:c.1598-883T>C	XP_024304083.1:n.1598-883T>C
XM_024448316.1:c.1559-883T>C	XP_024304084.1:n.1559-883T>C
XM_024448317.1:c.1559-883T>C	XP_024304085.1:n.1559-883T>C
XM_024448318.1:c.2441-883T>C	XP_024304086.1:n.2441-883T>C
XM_024448319.1:c.2384-883T>C	XP_024304087.1:n.2384-883T>C
NM_001008493.3:c.914-883T>C	NP_001008493.1:n.914-883T>C
NM_001377481.1:c.971-883T>C	NP_001364410.1:n.971-883T>C
NM_001377482.1:c.971-883T>C	NP_001364411.1:n.971-883T>C
NM_001377483.1:c.803-883T>C	NP_001364412.1:n.803-883T>C
NM_018212.6:c.914-883T>C MANE Select	NP_060682.2:n.914-883T>C