Canonical Allele Identifier: CA190540009

Gene: FOCAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.20715278G>T , CM000671.2:g.20715278G>T	GRCh38
NC_000009.11:g.20715277G>T , CM000671.1:g.20715277G>T	GRCh37
NC_000009.10:g.20705277G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001375567.1:c.-32-44G>T MANE Select	NP_001362496.1:n.-32-44G>T
ENST00000338382.11:c.-32-44G>T MANE Select	ENSP00000344307.6:n.-32-44G>T
NM_001375568.1:c.-32-44G>T	NP_001362497.1:n.-32-44G>T
NM_001375570.1:c.-32-44G>T	NP_001362499.1:n.-32-44G>T
NM_017794.4:c.-32-44G>T	NP_060264.4:n.-32-44G>T
NM_017794.5:c.-32-44G>T	NP_060264.4:n.-32-44G>T
ENST00000380249.5:c.-32-44G>T	ENSP00000369599.1:n.-32-44G>T
ENST00000604036.1:n.317-44G>T
XM_005251494.3:c.-32-44G>T	XP_005251551.2:n.-32-44G>T
XM_005251494.4:c.-32-44G>T	XP_005251551.2:n.-32-44G>T
XM_011517945.1:c.-32-44G>T	XP_011516247.1:n.-32-44G>T
XM_011517945.2:c.-32-44G>T	XP_011516247.1:n.-32-44G>T
XM_017014852.1:c.-32-44G>T	XP_016870341.1:n.-32-44G>T
XM_017014853.1:c.-32-44G>T	XP_016870342.1:n.-32-44G>T
XM_017014854.1:c.-32-44G>T	XP_016870343.1:n.-32-44G>T
XM_017014855.1:c.-32-44G>T	XP_016870344.1:n.-32-44G>T
XM_017014856.1:c.-32-44G>T	XP_016870345.1:n.-32-44G>T
XM_017014857.2:c.-32-44G>T	XP_016870346.1:n.-32-44G>T
XM_017014858.2:c.-32-44G>T	XP_016870347.1:n.-32-44G>T
XM_024447585.1:c.-32-44G>T	XP_024303353.1:n.-32-44G>T