Canonical Allele Identifier: CA398979582

Gene: ADAP2

Linked Data

• dbSNP Id: rs1452393581
• gnomAD v3: 17-30956445-C-T
• gnomAD v4: 17-30956445-C-T
• MyVariant Identifiers: chr17:g.29283463C>T (hg19) ; chr17:g.30956445C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956445C>T , CM000679.2:g.30956445C>T	GRCh38
NC_000017.10:g.29283463C>T , CM000679.1:g.29283463C>T	GRCh37
NC_000017.9:g.26307589C>T	NCBI36
NG_051975.1:g.39710C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1087C>T MANE Select	ENSP00000329468.3:p.Pro363Ser
ENST00000330889.7:c.1087C>T	ENSP00000329468.3:p.Pro363Ser
ENST00000470962.1:n.507C>T
ENST00000480980.1:n.521C>T
ENST00000580525.5:c.1105C>T	ENSP00000464121.1:p.Pro369Ser
ENST00000584828.5:c.402+54C>T
ENST00000585130.5:c.*686C>T	ENSP00000464120.1:n.*686C>T
NM_018404.2:c.1087C>T	NP_060874.1:p.Pro363Ser
XM_005258008.2:c.1105C>T	XP_005258065.1:p.Pro369Ser
XM_005258011.2:c.1042C>T	XP_005258068.1:p.Pro348Ser
XM_006721973.2:c.1051+54C>T	XP_006722036.1:n.1051+54C>T
XM_011524993.1:c.1102C>T	XP_011523295.1:p.Pro368Ser
XM_011524994.1:c.1084C>T	XP_011523296.1:p.Pro362Ser
NM_001346712.1:c.1105C>T	NP_001333641.1:p.Pro369Ser
NM_001346714.1:c.1084C>T	NP_001333643.1:p.Pro362Ser
NM_001346716.1:c.1033+54C>T	NP_001333645.1:n.1033+54C>T
NR_144488.1:n.1286C>T
XM_024450831.1:c.1087C>T	XP_024306599.1:p.Pro363Ser
XM_024450832.1:c.1102C>T	XP_024306600.1:p.Pro368Ser
XM_024450833.1:c.1042C>T	XP_024306601.1:p.Pro348Ser
XM_024450834.1:c.1051+54C>T	XP_024306602.1:n.1051+54C>T
XM_024450835.1:c.721C>T	XP_024306603.1:p.Pro241Ser
NM_018404.3:c.1087C>T MANE Select	NP_060874.1:p.Pro363Ser
NM_001346712.2:c.1105C>T	NP_001333641.1:p.Pro369Ser
NM_001346714.2:c.1084C>T	NP_001333643.1:p.Pro362Ser
NM_001346716.2:c.1033+54C>T	NP_001333645.1:n.1033+54C>T
NR_144488.2:n.1077C>T