Canonical Allele Identifier: CA2957766115

Gene: ABCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104831701_104831702insTGA , CM000671.2:g.104831701_104831702insTGA	GRCh38
NC_000009.11:g.107593982_107593983insTGA , CM000671.1:g.107593982_107593983insTGA	GRCh37
NC_000009.10:g.106633803_106633804insTGA	NCBI36
NG_007981.1:g.101454_101455insTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.1635_1636insTCA MANE Select	ENSP00000363868.3:p.Ser545_Ile546insSer
ENST00000678995.1:c.1635_1636insTCA	ENSP00000504612.1:p.Ser545_Ile546insSer
ENST00000374736.7:c.1635_1636insTCA	ENSP00000363868.3:p.Ser545_Ile546insSer
NM_005502.3:c.1635_1636insTCA	NP_005493.2:p.Ser545_Ile546insSer
XM_005251773.1:c.1635_1636insTCA	XP_005251830.1:p.Ser545_Ile546insSer
XM_005251776.1:c.1455_1456insTCA	XP_005251833.1:p.Ser485_Ile486insSer
XM_011518339.1:c.1710_1711insTCA	XP_011516641.1:p.Ser570_Ile571insSer
XM_011518340.1:c.1710_1711insTCA	XP_011516642.1:p.Ser570_Ile571insSer
XM_011518341.1:c.1710_1711insTCA	XP_011516643.1:p.Ser570_Ile571insSer
XM_011518342.1:c.1272_1273insTCA	XP_011516644.1:p.Ser424_Ile425insSer
XM_011518343.1:c.1710_1711insTCA	XP_011516645.1:p.Ser570_Ile571insSer
XM_011518344.1:c.1710_1711insTCA	XP_011516646.1:p.Ser570_Ile571insSer
XM_005251773.3:c.1635_1636insTCA	XP_005251830.1:p.Ser545_Ile546insSer
XM_005251776.3:c.1455_1456insTCA	XP_005251833.1:p.Ser485_Ile486insSer
XM_011518339.3:c.1710_1711insTCA	XP_011516641.1:p.Ser570_Ile571insSer
XM_011518340.3:c.1710_1711insTCA	XP_011516642.1:p.Ser570_Ile571insSer
XM_011518341.3:c.1710_1711insTCA	XP_011516643.1:p.Ser570_Ile571insSer
XM_011518342.3:c.1272_1273insTCA	XP_011516644.1:p.Ser424_Ile425insSer
XM_011518344.2:c.1710_1711insTCA	XP_011516646.1:p.Ser570_Ile571insSer
XM_017014378.2:c.1710_1711insTCA	XP_016869867.1:p.Ser570_Ile571insSer
XM_017014379.2:c.1710_1711insTCA	XP_016869868.1:p.Ser570_Ile571insSer
XM_017014380.2:c.1710_1711insTCA	XP_016869869.1:p.Ser570_Ile571insSer
XM_017014381.2:c.1710_1711insTCA	XP_016869870.1:p.Ser570_Ile571insSer
XM_017014382.2:c.1572_1573insTCA	XP_016869871.1:p.Ser524_Ile525insSer
XR_001746223.1:n.2023_2024insTCA
NM_005502.4:c.1635_1636insTCA MANE Select	NP_005493.2:p.Ser545_Ile546insSer