Canonical Allele Identifier: CA2670966594

Gene: ALB

Linked Data

• gnomAD v4: 4-73419490-T-TTTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419494_73419498dup , CM000666.2:g.73419494_73419498dup	GRCh38
NC_000004.11:g.74285211_74285215dup , CM000666.1:g.74285211_74285215dup	GRCh37
NC_000004.10:g.74504075_74504079dup	NCBI36
NG_009291.1:g.20240_20244dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1653-13_1653-9dup MANE Select	ENSP00000295897.4:n.1653-13_1653-9dup
ENST00000295897.8:c.1653-13_1653-9dup	ENSP00000295897.4:n.1653-13_1653-9dup
ENST00000401494.7:c.1308-13_1308-9dup	ENSP00000384695.3:n.1308-13_1308-9dup
ENST00000415165.6:c.1077-13_1077-9dup	ENSP00000401820.2:n.1077-13_1077-9dup
ENST00000476441.6:c.*932-13_*932-9dup	ENSP00000423727.1:n.*932-13_*932-9dup
ENST00000486939.1:n.307-13_307-9dup
ENST00000503124.5:c.1203-13_1203-9dup	ENSP00000421027.1:n.1203-13_1203-9dup
ENST00000505649.5:n.1200-13_1200-9dup
ENST00000508932.5:n.175+39_175+43dup
ENST00000509063.5:c.1653-13_1653-9dup	ENSP00000422784.1:n.1653-13_1653-9dup
ENST00000511370.1:c.1186-13_1186-9dup
ENST00000621085.4:c.1014-13_1014-9dup	ENSP00000483421.1:n.1014-13_1014-9dup
ENST00000621628.4:c.1014-13_1014-9dup	ENSP00000480485.1:n.1014-13_1014-9dup
NM_000477.5:c.1653-13_1653-9dup	NP_000468.1:n.1653-13_1653-9dup
NM_000477.6:c.1653-13_1653-9dup	NP_000468.1:n.1653-13_1653-9dup
NM_000477.7:c.1653-13_1653-9dup MANE Select	NP_000468.1:n.1653-13_1653-9dup