Canonical Allele Identifier: CA13821422

Gene: TMTC4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100624630A>G , CM000675.2:g.100624630A>G	GRCh38
NC_000013.10:g.101276884A>G , CM000675.1:g.101276884A>G	GRCh37
NC_000013.9:g.100074885A>G	NCBI36
NG_053145.1:g.55464T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342624.10:c.1836+905T>C MANE Select	ENSP00000343871.5:n.1836+905T>C
ENST00000328767.9:c.1446+905T>C	ENSP00000365409.2:n.1446+905T>C
ENST00000342624.9:c.1836+905T>C	ENSP00000343871.5:n.1836+905T>C
ENST00000376234.7:c.1779+905T>C	ENSP00000365408.3:n.1779+905T>C
NM_001079669.2:c.1779+905T>C	NP_001073137.1:n.1779+905T>C
NM_001286453.1:c.1446+905T>C	NP_001273382.1:n.1446+905T>C
NM_032813.3:c.1836+905T>C	NP_116202.2:n.1836+905T>C
XM_011521121.1:c.2010+905T>C	XP_011519423.1:n.2010+905T>C
XM_011521122.1:c.2010+905T>C	XP_011519424.1:n.2010+905T>C
XM_011521123.1:c.1953+905T>C	XP_011519425.1:n.1953+905T>C
XM_011521124.1:c.1953+905T>C	XP_011519426.1:n.1953+905T>C
XM_011521125.1:c.2010+905T>C	XP_011519427.1:n.2010+905T>C
XM_011521126.1:c.1302+905T>C	XP_011519428.1:n.1302+905T>C
XM_011521127.1:c.1128+905T>C	XP_011519429.1:n.1128+905T>C
NM_001079669.3:c.1779+905T>C	NP_001073137.1:n.1779+905T>C
NM_001286453.2:c.1446+905T>C	NP_001273382.1:n.1446+905T>C
NM_001350571.1:c.2010+905T>C	NP_001337500.1:n.2010+905T>C
NM_001350572.1:c.1779+905T>C	NP_001337501.1:n.1779+905T>C
NM_001350574.1:c.1953+905T>C	NP_001337503.1:n.1953+905T>C
NM_001350576.1:c.1830+905T>C	NP_001337505.1:n.1830+905T>C
NM_001350577.1:c.1773+905T>C	NP_001337506.1:n.1773+905T>C
NM_032813.4:c.1836+905T>C	NP_116202.2:n.1836+905T>C
NR_146794.1:n.2025+905T>C
XM_011521122.3:c.2010+905T>C	XP_011519424.1:n.2010+905T>C
XM_011521123.2:c.1953+905T>C	XP_011519425.1:n.1953+905T>C
XM_017020797.2:c.1302+905T>C	XP_016876286.1:n.1302+905T>C
XM_017020798.1:c.1128+905T>C	XP_016876287.1:n.1128+905T>C
XM_017020799.2:c.1128+905T>C	XP_016876288.1:n.1128+905T>C
NM_001079669.4:c.1779+905T>C	NP_001073137.1:n.1779+905T>C
NM_001286453.3:c.1446+905T>C	NP_001273382.1:n.1446+905T>C
NM_001350571.2:c.2010+905T>C	NP_001337500.1:n.2010+905T>C
NM_001350572.2:c.1779+905T>C	NP_001337501.1:n.1779+905T>C
NM_001350574.2:c.1953+905T>C	NP_001337503.1:n.1953+905T>C
NM_001350576.2:c.1830+905T>C	NP_001337505.1:n.1830+905T>C
NM_001350577.2:c.1773+905T>C	NP_001337506.1:n.1773+905T>C
NM_032813.5:c.1836+905T>C MANE Select	NP_116202.2:n.1836+905T>C
NR_146794.2:n.1885+905T>C