Canonical Allele Identifier: CA1345759058

Gene: VGLL4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.11583940C>G , CM000665.2:g.11583940C>G	GRCh38
NC_000003.11:g.11625414C>G , CM000665.1:g.11625414C>G	GRCh37
NC_000003.10:g.11600414C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430365.7:c.272+17893G>C MANE Select	ENSP00000404251.2:n.272+17893G>C
ENST00000273038.7:c.254+17893G>C	ENSP00000273038.3:n.254+17893G>C
ENST00000413604.5:c.77+17893G>C	ENSP00000404624.1:n.77+17893G>C
ENST00000417206.6:c.254+17893G>C	ENSP00000391932.2:n.254+17893G>C
ENST00000417466.5:c.269+17893G>C	ENSP00000411670.2:n.269+17893G>C
ENST00000418000.5:c.254+17893G>C	ENSP00000394439.1:n.254+17893G>C
ENST00000419541.4:c.254+17893G>C	ENSP00000395557.1:n.254+17893G>C
ENST00000424709.5:c.77+17893G>C	ENSP00000391554.1:n.77+17893G>C
ENST00000426568.5:c.269+17893G>C	ENSP00000413030.2:n.269+17893G>C
ENST00000430365.6:c.272+17893G>C	ENSP00000404251.2:n.272+17893G>C
ENST00000437722.1:c.77+17893G>C	ENSP00000393100.1:n.77+17893G>C
ENST00000445411.5:c.254+17893G>C	ENSP00000412923.1:n.254+17893G>C
ENST00000458499.5:c.242+17893G>C	ENSP00000394123.1:n.242+17893G>C
NM_001128219.2:c.272+17893G>C	NP_001121691.1:n.272+17893G>C
NM_001284390.1:c.269+17893G>C	NP_001271319.1:n.269+17893G>C
NM_001284391.1:c.77+17893G>C	NP_001271320.1:n.77+17893G>C
NM_014667.3:c.254+17893G>C	NP_055482.2:n.254+17893G>C
XM_011534267.1:c.257+17893G>C	XP_011532569.1:n.257+17893G>C
XM_011534268.1:c.77+17893G>C	XP_011532570.1:n.77+17893G>C
XM_011534269.1:c.77+17893G>C	XP_011532571.1:n.77+17893G>C
XM_011534270.1:c.272+17893G>C	XP_011532572.1:n.272+17893G>C
XM_011534267.2:c.257+17893G>C	XP_011532569.1:n.257+17893G>C
XM_017007541.1:c.269+17893G>C	XP_016863030.1:n.269+17893G>C
XM_017007542.1:c.254+17893G>C	XP_016863031.1:n.254+17893G>C
XM_024453835.1:c.254+17893G>C	XP_024309603.1:n.254+17893G>C
XM_024453836.1:c.254+17893G>C	XP_024309604.1:n.254+17893G>C
XM_024453837.1:c.254+17893G>C	XP_024309605.1:n.254+17893G>C
NM_001128219.3:c.272+17893G>C MANE Select	NP_001121691.1:n.272+17893G>C
NM_001284390.2:c.269+17893G>C	NP_001271319.1:n.269+17893G>C
NM_014667.4:c.254+17893G>C	NP_055482.2:n.254+17893G>C