Canonical Allele Identifier: CA1345787028

Gene: VGLL4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.11652993T>G , CM000665.2:g.11652993T>G	GRCh38
NC_000003.11:g.11694467T>G , CM000665.1:g.11694467T>G	GRCh37
NC_000003.10:g.11669467T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273038.7:c.64+49978A>C	ENSP00000273038.3:n.64+49978A>C
ENST00000417206.6:c.64+49978A>C	ENSP00000391932.2:n.64+49978A>C
ENST00000417466.5:c.79+18269A>C	ENSP00000411670.2:n.79+18269A>C
ENST00000418000.5:c.64+49978A>C	ENSP00000394439.1:n.64+49978A>C
ENST00000419541.4:c.64+49978A>C	ENSP00000395557.1:n.64+49978A>C
ENST00000426568.5:c.79+18269A>C	ENSP00000413030.2:n.79+18269A>C
ENST00000445411.5:c.64+49978A>C	ENSP00000412923.1:n.64+49978A>C
ENST00000623028.1:c.64+49978A>C	ENSP00000485472.1:n.64+49978A>C
NM_001284390.1:c.79+18269A>C	NP_001271319.1:n.79+18269A>C
NM_014667.3:c.64+49978A>C	NP_055482.2:n.64+49978A>C
XM_011534267.1:c.67+18281A>C	XP_011532569.1:n.67+18281A>C
XM_011534267.2:c.67+18281A>C	XP_011532569.1:n.67+18281A>C
XM_017007541.1:c.79+18269A>C	XP_016863030.1:n.79+18269A>C
XM_017007542.1:c.64+49978A>C	XP_016863031.1:n.64+49978A>C
XM_024453835.1:c.64+49978A>C	XP_024309603.1:n.64+49978A>C
XM_024453836.1:c.64+49978A>C	XP_024309604.1:n.64+49978A>C
XM_024453837.1:c.64+49978A>C	XP_024309605.1:n.64+49978A>C
NM_001284390.2:c.79+18269A>C	NP_001271319.1:n.79+18269A>C
NM_014667.4:c.64+49978A>C	NP_055482.2:n.64+49978A>C