Canonical Allele Identifier: CA341689976

Gene: AP4B1

Linked Data

• MyVariant Identifiers: chr1:g.114445326C>G (hg19) ; chr1:g.113902704C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113902704C>G , CM000663.2:g.113902704C>G	GRCh38
NC_000001.10:g.114445326C>G , CM000663.1:g.114445326C>G	GRCh37
NC_000001.9:g.114246849C>G	NCBI36
NG_031901.1:g.7416G>C
NG_057565.1:g.3086C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.114-819G>C	ENSP00000358577.2:n.114-819G>C
ENST00000369567.6:c.113+1901G>C	ENSP00000358580.1:n.113+1901G>C
ENST00000369571.3:c.272G>C	ENSP00000358584.3:p.Cys91Ser
ENST00000432415.6:c.113+1901G>C	ENSP00000393622.2:n.113+1901G>C
ENST00000460653.2:c.272G>C	ENSP00000518881.1:p.Cys91Ser
ENST00000484201.6:c.114-819G>C	ENSP00000518883.1:n.114-819G>C
ENST00000489092.6:c.144G>C	ENSP00000518884.1:p.Val48=
ENST00000489499.6:c.272G>C	ENSP00000518882.1:p.Cys91Ser
ENST00000713588.1:c.272G>C	ENSP00000518880.1:p.Cys91Ser
ENST00000713590.1:c.272G>C	ENSP00000518886.1:p.Cys91Ser
ENST00000369569.6:c.272G>C MANE Select	ENSP00000358582.1:p.Cys91Ser
ENST00000256658.8:c.272G>C	ENSP00000256658.4:p.Cys91Ser
ENST00000369564.5:c.114-819G>C	ENSP00000358577.1:n.114-819G>C
ENST00000369567.5:c.113+1901G>C	ENSP00000358580.1:n.113+1901G>C
ENST00000369569.5:c.272G>C	ENSP00000358582.1:p.Cys91Ser
ENST00000369571.2:c.272G>C	ENSP00000358584.2:p.Cys91Ser
ENST00000432415.5:c.113+1901G>C	ENSP00000393622.1:n.113+1901G>C
ENST00000484201.5:n.305-819G>C
ENST00000489092.5:n.271G>C
ENST00000489499.5:n.388G>C
NM_001253852.1:c.272G>C	NP_001240781.1:p.Cys91Ser
NM_001253852.2:c.272G>C	NP_001240781.1:p.Cys91Ser
NM_001253853.1:c.-26G>C	NP_001240782.1:n.-26G>C
NM_001253853.2:c.-26G>C	NP_001240782.1:n.-26G>C
NM_001308312.1:c.113+1901G>C	NP_001295241.1:n.113+1901G>C
NM_006594.3:c.272G>C	NP_006585.2:p.Cys91Ser
NM_006594.4:c.272G>C	NP_006585.2:p.Cys91Ser
XM_005270381.2:c.272G>C	XP_005270438.1:p.Cys91Ser
XM_005270382.3:c.272G>C	XP_005270439.1:p.Cys91Ser
XM_011540523.1:c.114-819G>C	XP_011538825.1:n.114-819G>C
XM_011540524.1:c.114-819G>C	XP_011538826.1:n.114-819G>C
XM_011540525.1:c.272G>C	XP_011538827.1:p.Cys91Ser
XM_011540527.1:c.-199G>C	XP_011538829.1:n.-199G>C
XR_246227.1:n.454G>C
XR_246228.2:n.454G>C
XM_011540523.3:c.114-819G>C	XP_011538825.1:n.114-819G>C
XM_011540525.3:c.272G>C	XP_011538827.1:p.Cys91Ser
XM_017000089.2:c.272G>C	XP_016855578.1:p.Cys91Ser
XM_017000090.1:c.113+1901G>C	XP_016855579.1:n.113+1901G>C
XM_017000091.2:c.272G>C	XP_016855580.1:p.Cys91Ser
XM_017000092.2:c.-973G>C	XP_016855581.1:n.-973G>C
XM_017000093.2:c.272G>C	XP_016855582.1:p.Cys91Ser
XM_024452422.1:c.272G>C	XP_024308190.1:p.Cys91Ser
XM_024452423.1:c.272G>C	XP_024308191.1:p.Cys91Ser
XM_024452435.1:c.114-819G>C	XP_024308203.1:n.114-819G>C
XM_024452441.1:c.113+1901G>C	XP_024308209.1:n.113+1901G>C
XR_001736928.2:n.474G>C
XR_001736930.2:n.474G>C
XR_002958805.1:n.474G>C
XR_002958806.1:n.474G>C
XR_002958807.1:n.354G>C
NM_001253852.3:c.272G>C MANE Select	NP_001240781.1:p.Cys91Ser
NM_001253853.3:c.-26G>C	NP_001240782.1:n.-26G>C
NM_001308312.2:c.113+1901G>C	NP_001295241.1:n.113+1901G>C
NM_006594.5:c.272G>C	NP_006585.2:p.Cys91Ser