Canonical Allele Identifier: CA1468148692

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420124_73420125delinsTA , CM000666.2:g.73420124_73420125delinsTA	GRCh38
NC_000004.11:g.74285841_74285842delinsTA , CM000666.1:g.74285841_74285842delinsTA	GRCh37
NC_000004.10:g.74504705_74504706delinsTA	NCBI36
NG_009291.1:g.20870_20871delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-130_1786-129delinsTA MANE Select	ENSP00000295897.4:n.1786-130_1786-129delinsTA
ENST00000295897.8:c.1786-130_1786-129delinsTA	ENSP00000295897.4:n.1786-130_1786-129delinsTA
ENST00000401494.7:c.1441-130_1441-129delinsTA	ENSP00000384695.3:n.1441-130_1441-129delinsTA
ENST00000415165.6:c.1210-130_1210-129delinsTA	ENSP00000401820.2:n.1210-130_1210-129delinsTA
ENST00000476441.6:c.*1065-130_*1065-129delinsTA	ENSP00000423727.1:n.*1065-130_*1065-129delinsTA
ENST00000495173.1:n.94-130_94-129delinsTA
ENST00000503124.5:c.1336-130_1336-129delinsTA	ENSP00000421027.1:n.1336-130_1336-129delinsTA
ENST00000505649.5:n.1333-130_1333-129delinsTA
ENST00000508932.5:n.176-130_176-129delinsTA
ENST00000509063.5:c.1785+485_1785+486delinsTA	ENSP00000422784.1:n.1785+485_1785+486delinsTA
ENST00000511370.1:c.1319-130_1319-129delinsTA
ENST00000621085.4:c.1147-130_1147-129delinsTA	ENSP00000483421.1:n.1147-130_1147-129delinsTA
ENST00000621628.4:c.1147-130_1147-129delinsTA	ENSP00000480485.1:n.1147-130_1147-129delinsTA
NM_000477.5:c.1786-130_1786-129delinsTA	NP_000468.1:n.1786-130_1786-129delinsTA
NM_000477.6:c.1786-130_1786-129delinsTA	NP_000468.1:n.1786-130_1786-129delinsTA
NM_000477.7:c.1786-130_1786-129delinsTA MANE Select	NP_000468.1:n.1786-130_1786-129delinsTA