Canonical Allele Identifier: CA2670966556

Gene: ALB

Linked Data

• gnomAD v4: 4-73419452-ATACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419454_73419457del , CM000666.2:g.73419454_73419457del	GRCh38
NC_000004.11:g.74285171_74285174del , CM000666.1:g.74285171_74285174del	GRCh37
NC_000004.10:g.74504035_74504038del	NCBI36
NG_009291.1:g.20200_20203del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1653-53_1653-50del MANE Select	ENSP00000295897.4:n.1653-53_1653-50del
ENST00000295897.8:c.1653-53_1653-50del	ENSP00000295897.4:n.1653-53_1653-50del
ENST00000401494.7:c.1308-53_1308-50del	ENSP00000384695.3:n.1308-53_1308-50del
ENST00000415165.6:c.1077-53_1077-50del	ENSP00000401820.2:n.1077-53_1077-50del
ENST00000476441.6:c.*932-53_*932-50del	ENSP00000423727.1:n.*932-53_*932-50del
ENST00000486939.1:n.307-53_307-50del
ENST00000503124.5:c.1203-53_1203-50del	ENSP00000421027.1:n.1203-53_1203-50del
ENST00000505649.5:n.1200-53_1200-50del
ENST00000508932.5:n.174_175+2del
ENST00000509063.5:c.1653-53_1653-50del	ENSP00000422784.1:n.1653-53_1653-50del
ENST00000511370.1:c.1186-53_1186-50del
ENST00000621085.4:c.1014-53_1014-50del	ENSP00000483421.1:n.1014-53_1014-50del
ENST00000621628.4:c.1014-53_1014-50del	ENSP00000480485.1:n.1014-53_1014-50del
NM_000477.5:c.1653-53_1653-50del	NP_000468.1:n.1653-53_1653-50del
NM_000477.6:c.1653-53_1653-50del	NP_000468.1:n.1653-53_1653-50del
NM_000477.7:c.1653-53_1653-50del MANE Select	NP_000468.1:n.1653-53_1653-50del