Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017631A>G , CM000674.2:g.10017631A>G	GRCh38
NC_000012.11:g.10170230A>G , CM000674.1:g.10170230A>G	GRCh37
NC_000012.10:g.10061497A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-700A>G MANE Select	ENSP00000344563.5:n.681-700A>G
ENST00000338896.10:c.681-700A>G	ENSP00000344563.5:n.681-700A>G
ENST00000338896.9:c.681-700A>G	ENSP00000344563.5:n.681-700A>G
ENST00000396502.5:c.*1885A>G	ENSP00000379759.1:n.*1885A>G
ENST00000539155.1:c.*2378A>G	ENSP00000444909.1:n.*2378A>G
ENST00000544853.5:c.*129-700A>G	ENSP00000439561.1:n.*129-700A>G
NM_001129998.1:c.681-700A>G	NP_001123470.1:n.681-700A>G
NM_205852.2:c.*1885A>G	NP_995324.2:n.*1885A>G
NR_120484.1:n.249-1858T>C
XM_006719070.2:c.681-787A>G	XP_006719133.1:n.681-787A>G
XM_006719071.2:c.*3-700A>G	XP_006719134.1:n.*3-700A>G
XM_006719072.1:c.*658A>G	XP_006719135.1:n.*658A>G
XM_011520658.1:c.654-700A>G	XP_011518960.1:n.654-700A>G
XM_011520659.1:c.*634A>G	XP_011518961.1:n.*634A>G
XM_011520660.1:c.*629A>G	XP_011518962.1:n.*629A>G
XM_011520661.1:c.*10-700A>G	XP_011518963.1:n.*10-700A>G
XM_011520662.1:c.*665A>G	XP_011518964.1:n.*665A>G
XM_011520663.1:c.526-700A>G	XP_011518965.1:n.526-700A>G
XM_011520664.1:c.526-787A>G	XP_011518966.1:n.526-787A>G
XR_242889.3:n.956-700A>G
XR_931290.1:n.1611A>G
NM_001129998.2:c.681-700A>G	NP_001123470.1:n.681-700A>G
NM_001319241.1:c.372-700A>G	NP_001306170.1:n.372-700A>G
NM_001319242.1:c.*1885A>G	NP_001306171.1:n.*1885A>G
NM_205852.3:c.*1885A>G	NP_995324.2:n.*1885A>G
NR_135049.1:n.961-700A>G
XM_011520658.2:c.654-700A>G	XP_011518960.1:n.654-700A>G
XM_011520663.2:c.526-700A>G	XP_011518965.1:n.526-700A>G
XM_017019295.1:c.372-700A>G	XP_016874784.1:n.372-700A>G
XM_024448976.1:c.681-787A>G	XP_024304744.1:n.681-787A>G
XM_024448977.1:c.*1892A>G	XP_024304745.1:n.*1892A>G
XR_002957401.1:n.106-1483T>C
NM_001129998.3:c.681-700A>G MANE Select	NP_001123470.1:n.681-700A>G
NM_001387138.1:c.681-787A>G	NP_001374067.1:n.681-787A>G
NR_169587.1:n.258-1483T>C