Canonical Allele Identifier: CA648963738

Gene: ALB

Linked Data

• COSMIC: COSN1300887

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419925_73419938del , CM000666.2:g.73419925_73419938del	GRCh38
NC_000004.11:g.74285642_74285655del , CM000666.1:g.74285642_74285655del	GRCh37
NC_000004.10:g.74504506_74504519del	NCBI36
NG_009291.1:g.20671_20684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+286_1785+299del MANE Select	ENSP00000295897.4:n.1785+286_1785+299del
ENST00000295897.8:c.1785+286_1785+299del	ENSP00000295897.4:n.1785+286_1785+299del
ENST00000401494.7:c.1440+286_1440+299del	ENSP00000384695.3:n.1440+286_1440+299del
ENST00000415165.6:c.1209+286_1209+299del	ENSP00000401820.2:n.1209+286_1209+299del
ENST00000476441.6:c.*1064+286_*1064+299del	ENSP00000423727.1:n.*1064+286_*1064+299del
ENST00000495173.1:n.93+286_93+299del
ENST00000503124.5:c.1335+286_1335+299del	ENSP00000421027.1:n.1335+286_1335+299del
ENST00000505649.5:n.1332+286_1332+299del
ENST00000508932.5:n.176-329_176-316del
ENST00000509063.5:c.1785+286_1785+299del	ENSP00000422784.1:n.1785+286_1785+299del
ENST00000511370.1:c.1318+286_1318+299del
ENST00000621085.4:c.1146+286_1146+299del	ENSP00000483421.1:n.1146+286_1146+299del
ENST00000621628.4:c.1146+286_1146+299del	ENSP00000480485.1:n.1146+286_1146+299del
NM_000477.5:c.1785+286_1785+299del	NP_000468.1:n.1785+286_1785+299del
NM_000477.6:c.1785+286_1785+299del	NP_000468.1:n.1785+286_1785+299del
NM_000477.7:c.1785+286_1785+299del MANE Select	NP_000468.1:n.1785+286_1785+299del