Canonical Allele Identifier: CA471268853

Gene: TWNK

Linked Data

• MyVariant Identifiers: chr10:g.102748609A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988852A>C , CM000672.2:g.100988852A>C	GRCh38
NC_000010.10:g.102748609A>C , CM000672.1:g.102748609A>C	GRCh37
NC_000010.9:g.102738599A>C	NCBI36
NG_011646.1:g.3664T>G
NG_012624.1:g.6317A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000311916.8:c.642A>C MANE Select	ENSP00000309595.2:p.Ser214=
ENST00000370228.2:c.642A>C	ENSP00000359248.1:p.Ser214=
ENST00000643860.1:c.642A>C	ENSP00000494389.1:p.Ser214=
ENST00000646226.1:n.59-792A>C
ENST00000311916.6:c.642A>C	ENSP00000309595.2:p.Ser214=
ENST00000370228.1:c.642A>C	ENSP00000359248.1:p.Ser214=
ENST00000459764.1:n.87-792A>C
ENST00000473656.5:n.65-792A>C
ENST00000476766.5:n.192-854A>C
NM_001163812.1:c.642A>C	NP_001157284.1:p.Ser214=
NM_001163813.1:c.-119-792A>C	NP_001157285.1:n.-119-792A>C
NM_001163814.1:c.-119-792A>C	NP_001157286.1:n.-119-792A>C
NM_021830.4:c.642A>C	NP_068602.2:p.Ser214=
XM_011539975.1:c.-57-854A>C	XP_011538277.1:n.-57-854A>C
XR_945788.1:n.1475A>C
XM_011539975.2:c.-57-854A>C	XP_011538277.1:n.-57-854A>C
XM_017016437.1:c.-659A>C	XP_016871926.1:n.-659A>C
XR_001747142.1:n.816A>C
XR_001747144.1:n.816A>C
XR_002956991.1:n.816A>C
XR_945788.2:n.816A>C
NM_021830.5:c.642A>C MANE Select	NP_068602.2:p.Ser214=
NM_001163812.2:c.642A>C	NP_001157284.1:p.Ser214=
NM_001163813.2:c.-119-792A>C	NP_001157285.1:n.-119-792A>C
NM_001163814.2:c.-119-792A>C	NP_001157286.1:n.-119-792A>C
NM_001368275.1:c.-57-854A>C	NP_001355204.1:n.-57-854A>C
NR_160738.1:n.1310A>C
NR_160739.1:n.72-792A>C
NR_160740.1:n.1310A>C
NR_160741.1:n.1310A>C
NR_160742.1:n.1310A>C