Canonical Allele Identifier: CA378207652

Gene: TWNK

Linked Data

• MyVariant Identifiers: chr10:g.102748530A>C (hg19) ; chr10:g.100988773A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988773A>C , CM000672.2:g.100988773A>C	GRCh38
NC_000010.10:g.102748530A>C , CM000672.1:g.102748530A>C	GRCh37
NC_000010.9:g.102738520A>C	NCBI36
NG_011646.1:g.3743T>G
NG_012624.1:g.6238A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.563A>C MANE Select	ENSP00000309595.2:p.Asp188Ala
ENST00000370228.2:c.563A>C	ENSP00000359248.1:p.Asp188Ala
ENST00000643860.1:c.563A>C	ENSP00000494389.1:p.Asp188Ala
ENST00000646226.1:n.59-871A>C
ENST00000311916.6:c.563A>C	ENSP00000309595.2:p.Asp188Ala
ENST00000370228.1:c.563A>C	ENSP00000359248.1:p.Asp188Ala
ENST00000459764.1:n.87-871A>C
ENST00000473656.5:n.65-871A>C
ENST00000476766.5:n.192-933A>C
NM_001163812.1:c.563A>C	NP_001157284.1:p.Asp188Ala
NM_001163813.1:c.-119-871A>C	NP_001157285.1:n.-119-871A>C
NM_001163814.1:c.-119-871A>C	NP_001157286.1:n.-119-871A>C
NM_021830.4:c.563A>C	NP_068602.2:p.Asp188Ala
XM_011539975.1:c.-57-933A>C	XP_011538277.1:n.-57-933A>C
XR_945788.1:n.1396A>C
XM_011539975.2:c.-57-933A>C	XP_011538277.1:n.-57-933A>C
XM_017016437.1:c.-738A>C	XP_016871926.1:n.-738A>C
XR_001747142.1:n.737A>C
XR_001747144.1:n.737A>C
XR_002956991.1:n.737A>C
XR_945788.2:n.737A>C
NM_021830.5:c.563A>C MANE Select	NP_068602.2:p.Asp188Ala
NM_001163812.2:c.563A>C	NP_001157284.1:p.Asp188Ala
NM_001163813.2:c.-119-871A>C	NP_001157285.1:n.-119-871A>C
NM_001163814.2:c.-119-871A>C	NP_001157286.1:n.-119-871A>C
NM_001368275.1:c.-57-933A>C	NP_001355204.1:n.-57-933A>C
NR_160738.1:n.1231A>C
NR_160739.1:n.72-871A>C
NR_160740.1:n.1231A>C
NR_160741.1:n.1231A>C
NR_160742.1:n.1231A>C