Canonical Allele Identifier: CA2670966264

Gene: ALB

Linked Data

• gnomAD v4: 4-73418034-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418038del , CM000666.2:g.73418038del	GRCh38
NC_000004.11:g.74283755del , CM000666.1:g.74283755del	GRCh37
NC_000004.10:g.74502619del	NCBI36
NG_009291.1:g.18784del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1429-50del MANE Select	ENSP00000295897.4:n.1429-50del
ENST00000295897.8:c.1429-50del	ENSP00000295897.4:n.1429-50del
ENST00000401494.7:c.1084-50del	ENSP00000384695.3:n.1084-50del
ENST00000415165.6:c.853-50del	ENSP00000401820.2:n.853-50del
ENST00000476441.6:c.*708-50del	ENSP00000423727.1:n.*708-50del
ENST00000486939.1:n.33del
ENST00000503124.5:c.979-50del	ENSP00000421027.1:n.979-50del
ENST00000505649.5:n.976-50del
ENST00000509063.5:c.1429-50del	ENSP00000422784.1:n.1429-50del
ENST00000511370.1:c.962-50del
ENST00000621085.4:c.790-50del	ENSP00000483421.1:n.790-50del
ENST00000621628.4:c.790-50del	ENSP00000480485.1:n.790-50del
NM_000477.5:c.1429-50del	NP_000468.1:n.1429-50del
NM_000477.6:c.1429-50del	NP_000468.1:n.1429-50del
NM_000477.7:c.1429-50del MANE Select	NP_000468.1:n.1429-50del