Canonical Allele Identifier: CA798250708

Gene: ALB

Linked Data

• dbSNP Id: rs1488984409
• gnomAD v3: 4-73419939-AATTT-A
• gnomAD v4: 4-73419939-AATTT-A
• MyVariant Identifiers: chr4:g.74285657_74285660del (hg19) ; chr4:g.73419940_73419943del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419945_73419948del , CM000666.2:g.73419945_73419948del	GRCh38
NC_000004.11:g.74285662_74285665del , CM000666.1:g.74285662_74285665del	GRCh37
NC_000004.10:g.74504526_74504529del	NCBI36
NG_009291.1:g.20691_20694del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+306_1786-306del MANE Select	ENSP00000295897.4:n.1785+306_1786-306del
ENST00000295897.8:c.1785+306_1786-306del	ENSP00000295897.4:n.1785+306_1786-306del
ENST00000401494.7:c.1440+306_1441-306del	ENSP00000384695.3:n.1440+306_1441-306del
ENST00000415165.6:c.1209+306_1210-306del	ENSP00000401820.2:n.1209+306_1210-306del
ENST00000476441.6:c.*1064+306_*1065-306del	ENSP00000423727.1:n.*1064+306_*1065-306del
ENST00000495173.1:n.93+306_94-306del
ENST00000503124.5:c.1335+306_1336-306del	ENSP00000421027.1:n.1335+306_1336-306del
ENST00000505649.5:n.1332+306_1333-306del
ENST00000508932.5:n.176-309_176-306del
ENST00000509063.5:c.1785+306_1785+309del	ENSP00000422784.1:n.1785+306_1785+309del
ENST00000511370.1:c.1318+306_1319-306del
ENST00000621085.4:c.1146+306_1147-306del	ENSP00000483421.1:n.1146+306_1147-306del
ENST00000621628.4:c.1146+306_1147-306del	ENSP00000480485.1:n.1146+306_1147-306del
NM_000477.5:c.1785+306_1786-306del	NP_000468.1:n.1785+306_1786-306del
NM_000477.6:c.1785+306_1786-306del	NP_000468.1:n.1785+306_1786-306del
NM_000477.7:c.1785+306_1786-306del MANE Select	NP_000468.1:n.1785+306_1786-306del