Canonical Allele Identifier: CA1468148551

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419879_73419880delinsTG , CM000666.2:g.73419879_73419880delinsTG	GRCh38
NC_000004.11:g.74285596_74285597delinsTG , CM000666.1:g.74285596_74285597delinsTG	GRCh37
NC_000004.10:g.74504460_74504461delinsTG	NCBI36
NG_009291.1:g.20625_20626delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+240_1785+241delinsTG MANE Select	ENSP00000295897.4:n.1785+240_1785+241delinsTG
ENST00000295897.8:c.1785+240_1785+241delinsTG	ENSP00000295897.4:n.1785+240_1785+241delinsTG
ENST00000401494.7:c.1440+240_1440+241delinsTG	ENSP00000384695.3:n.1440+240_1440+241delinsTG
ENST00000415165.6:c.1209+240_1209+241delinsTG	ENSP00000401820.2:n.1209+240_1209+241delinsTG
ENST00000476441.6:c.*1064+240_*1064+241delinsTG	ENSP00000423727.1:n.*1064+240_*1064+241delinsTG
ENST00000495173.1:n.93+240_93+241delinsTG
ENST00000503124.5:c.1335+240_1335+241delinsTG	ENSP00000421027.1:n.1335+240_1335+241delinsTG
ENST00000505649.5:n.1332+240_1332+241delinsTG
ENST00000508932.5:n.176-375_176-374delinsTG
ENST00000509063.5:c.1785+240_1785+241delinsTG	ENSP00000422784.1:n.1785+240_1785+241delinsTG
ENST00000511370.1:c.1318+240_1318+241delinsTG
ENST00000621085.4:c.1146+240_1146+241delinsTG	ENSP00000483421.1:n.1146+240_1146+241delinsTG
ENST00000621628.4:c.1146+240_1146+241delinsTG	ENSP00000480485.1:n.1146+240_1146+241delinsTG
NM_000477.5:c.1785+240_1785+241delinsTG	NP_000468.1:n.1785+240_1785+241delinsTG
NM_000477.6:c.1785+240_1785+241delinsTG	NP_000468.1:n.1785+240_1785+241delinsTG
NM_000477.7:c.1785+240_1785+241delinsTG MANE Select	NP_000468.1:n.1785+240_1785+241delinsTG