Canonical Allele Identifier: CA798286907

Gene: ALB

Linked Data

• dbSNP Id: rs1249607351
• gnomAD v3: 4-73409179-CT-C
• gnomAD v4: 4-73409179-CT-C
• MyVariant Identifiers: chr4:g.74274897del (hg19) ; chr4:g.73409180del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409185del , CM000666.2:g.73409185del	GRCh38
NC_000004.11:g.74274902del , CM000666.1:g.74274902del	GRCh37
NC_000004.10:g.74493766del	NCBI36
NG_009291.1:g.9931del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-170del MANE Select	ENSP00000295897.4:n.483-170del
ENST00000295897.8:c.483-170del	ENSP00000295897.4:n.483-170del
ENST00000401494.7:c.138-170del	ENSP00000384695.3:n.138-170del
ENST00000415165.6:c.138-2811del	ENSP00000401820.2:n.138-2811del
ENST00000441319.5:c.489-170del	ENSP00000392541.1:n.489-170del
ENST00000476441.6:c.80-170del	ENSP00000423727.1:n.80-170del
ENST00000503124.5:c.33-170del	ENSP00000421027.1:n.33-170del
ENST00000505649.5:n.169-170del
ENST00000509063.5:c.483-170del	ENSP00000422784.1:n.483-170del
ENST00000514786.1:n.452-170del
ENST00000621085.4:c.483-170del	ENSP00000483421.1:n.483-170del
ENST00000621628.4:c.486+109del	ENSP00000480485.1:n.486+109del
NM_000477.5:c.483-170del	NP_000468.1:n.483-170del
NM_000477.6:c.483-170del	NP_000468.1:n.483-170del
NM_000477.7:c.483-170del MANE Select	NP_000468.1:n.483-170del