Canonical Allele Identifier: CA2529582711

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419887_73419898del , CM000666.2:g.73419887_73419898del	GRCh38
NC_000004.11:g.74285604_74285615del , CM000666.1:g.74285604_74285615del	GRCh37
NC_000004.10:g.74504468_74504479del	NCBI36
NG_009291.1:g.20633_20644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+248_1785+259del MANE Select	ENSP00000295897.4:n.1785+248_1785+259del
ENST00000295897.8:c.1785+248_1785+259del	ENSP00000295897.4:n.1785+248_1785+259del
ENST00000401494.7:c.1440+248_1440+259del	ENSP00000384695.3:n.1440+248_1440+259del
ENST00000415165.6:c.1209+248_1209+259del	ENSP00000401820.2:n.1209+248_1209+259del
ENST00000476441.6:c.*1064+248_*1064+259del	ENSP00000423727.1:n.*1064+248_*1064+259del
ENST00000495173.1:n.93+248_93+259del
ENST00000503124.5:c.1335+248_1335+259del	ENSP00000421027.1:n.1335+248_1335+259del
ENST00000505649.5:n.1332+248_1332+259del
ENST00000508932.5:n.176-367_176-356del
ENST00000509063.5:c.1785+248_1785+259del	ENSP00000422784.1:n.1785+248_1785+259del
ENST00000511370.1:c.1318+248_1318+259del
ENST00000621085.4:c.1146+248_1146+259del	ENSP00000483421.1:n.1146+248_1146+259del
ENST00000621628.4:c.1146+248_1146+259del	ENSP00000480485.1:n.1146+248_1146+259del
NM_000477.5:c.1785+248_1785+259del	NP_000468.1:n.1785+248_1785+259del
NM_000477.6:c.1785+248_1785+259del	NP_000468.1:n.1785+248_1785+259del
NM_000477.7:c.1785+248_1785+259del MANE Select	NP_000468.1:n.1785+248_1785+259del