Canonical Allele Identifier: CA14803260

Gene: ANGPT4

Linked Data

• dbSNP Id: rs2144151
• gnomAD v2: 20-883644-T-G
• gnomAD v3: 20-903001-T-G
• gnomAD v4: 20-903001-T-G
• MyVariant Identifiers: chr20:g.883644T>G (hg19) ; chr20:g.903001T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.903001T>G , CM000682.2:g.903001T>G	GRCh38
NC_000020.10:g.883644T>G , CM000682.1:g.883644T>G	GRCh37
NC_000020.9:g.831644T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381922.5:c.310-12633A>C MANE Select	ENSP00000371347.3:n.310-12633A>C
ENST00000381922.4:c.310-12633A>C	ENSP00000371347.3:n.310-12633A>C
NM_015985.2:c.310-12633A>C	NP_057069.1:n.310-12633A>C
XM_005260720.2:c.310-12633A>C	XP_005260777.1:n.310-12633A>C
XM_011529239.1:c.309+12905A>C	XP_011527541.1:n.309+12905A>C
XM_011529242.1:c.-58+4993A>C	XP_011527544.1:n.-58+4993A>C
XM_011529243.1:c.-58+4263A>C	XP_011527545.1:n.-58+4263A>C
NM_001322809.1:c.310-12633A>C	NP_001309738.1:n.310-12633A>C
NM_015985.3:c.310-12633A>C	NP_057069.1:n.310-12633A>C
XM_011529239.3:c.309+12905A>C	XP_011527541.1:n.309+12905A>C
NM_015985.4:c.310-12633A>C MANE Select	NP_057069.1:n.310-12633A>C
NM_001322809.2:c.310-12633A>C	NP_001309738.1:n.310-12633A>C