Canonical Allele Identifier: CA1468141814

Gene: ALB

Linked Data

• dbSNP Id: rs1718924452
• gnomAD v4: 4-73413279-GCAAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413282_73413285del , CM000666.2:g.73413282_73413285del	GRCh38
NC_000004.11:g.74278999_74279002del , CM000666.1:g.74278999_74279002del	GRCh37
NC_000004.10:g.74497863_74497866del	NCBI36
NG_009291.1:g.14028_14031del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-138_844-135del MANE Select	ENSP00000295897.4:n.844-138_844-135del
ENST00000295897.8:c.844-138_844-135del	ENSP00000295897.4:n.844-138_844-135del
ENST00000401494.7:c.499-138_499-135del	ENSP00000384695.3:n.499-138_499-135del
ENST00000415165.6:c.268-138_268-135del	ENSP00000401820.2:n.268-138_268-135del
ENST00000476441.6:c.*123-138_*123-135del	ENSP00000423727.1:n.*123-138_*123-135del
ENST00000484992.1:n.26_29del
ENST00000503124.5:c.394-138_394-135del	ENSP00000421027.1:n.394-138_394-135del
ENST00000505649.5:n.530-138_530-135del
ENST00000509063.5:c.844-138_844-135del	ENSP00000422784.1:n.844-138_844-135del
ENST00000511370.1:c.377-138_377-135del
ENST00000621085.4:c.491-1824_491-1821del	ENSP00000483421.1:n.491-1824_491-1821del
ENST00000621628.4:c.487-1820_487-1817del	ENSP00000480485.1:n.487-1820_487-1817del
NM_000477.5:c.844-138_844-135del	NP_000468.1:n.844-138_844-135del
NM_000477.6:c.844-138_844-135del	NP_000468.1:n.844-138_844-135del
NM_000477.7:c.844-138_844-135del MANE Select	NP_000468.1:n.844-138_844-135del