Canonical Allele Identifier: CA1468143498

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415095_73415096delinsTG , CM000666.2:g.73415095_73415096delinsTG	GRCh38
NC_000004.11:g.74280812_74280813delinsTG , CM000666.1:g.74280812_74280813delinsTG	GRCh37
NC_000004.10:g.74499676_74499677delinsTG	NCBI36
NG_009291.1:g.15841_15842delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1119_1120delinsTG MANE Select	ENSP00000295897.4:p.Leu373=
ENST00000295897.8:c.1119_1120delinsTG	ENSP00000295897.4:p.Leu373=
ENST00000401494.7:c.774_775delinsTG	ENSP00000384695.3:p.Leu258=
ENST00000415165.6:c.543_544delinsTG	ENSP00000401820.2:p.Leu181=
ENST00000476441.6:c.*398_*399delinsTG	ENSP00000423727.1:n.*398_*399delinsTG
ENST00000484992.1:n.439_440delinsTG
ENST00000503124.5:c.669_670delinsTG	ENSP00000421027.1:p.Leu223=
ENST00000504043.1:n.122_123delinsTG
ENST00000505649.5:n.805_806delinsTG
ENST00000509063.5:c.1119_1120delinsTG	ENSP00000422784.1:p.Leu373=
ENST00000511370.1:c.652_653delinsTG
ENST00000621085.4:c.491-11_491-10delinsTG	ENSP00000483421.1:n.491-11_491-10delinsTG
ENST00000621628.4:c.487-7_487-6delinsTG	ENSP00000480485.1:n.487-7_487-6delinsTG
NM_000477.5:c.1119_1120delinsTG	NP_000468.1:p.Leu373=
NM_000477.6:c.1119_1120delinsTG	NP_000468.1:p.Leu373=
NM_000477.7:c.1119_1120delinsTG MANE Select	NP_000468.1:p.Leu373=