Canonical Allele Identifier: CA121381380

Gene: ACOT12

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81359147T>A , CM000667.2:g.81359147T>A	GRCh38
NC_000005.9:g.80654966T>A , CM000667.1:g.80654966T>A	GRCh37
NC_000005.8:g.80690722T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307624.8:c.496+756A>T MANE Select	ENSP00000303246.3:n.496+756A>T
ENST00000307624.7:c.496+756A>T	ENSP00000303246.3:n.496+756A>T
NM_130767.2:c.496+756A>T	NP_570123.1:n.496+756A>T
XM_006714531.2:c.496+756A>T	XP_006714594.1:n.496+756A>T
XM_006714532.2:c.496+756A>T	XP_006714595.1:n.496+756A>T
XM_011543164.1:c.394+756A>T	XP_011541466.1:n.394+756A>T
XM_011543165.1:c.355+756A>T	XP_011541467.1:n.355+756A>T
XM_006714532.3:c.496+756A>T	XP_006714595.1:n.496+756A>T
XM_017009045.1:c.496+756A>T	XP_016864534.1:n.496+756A>T
XM_017009046.1:c.496+756A>T	XP_016864535.1:n.496+756A>T
XM_017009047.1:c.394+756A>T	XP_016864536.1:n.394+756A>T
XM_024454366.1:c.355+756A>T	XP_024310134.1:n.355+756A>T
NM_130767.3:c.496+756A>T MANE Select	NP_570123.1:n.496+756A>T