Canonical Allele Identifier: CA199040337

Gene: ASTN2 ASTN2-AS1

Linked Data

• dbSNP Id: rs41266663
• gnomAD v3: 9-116552014-C-T
• gnomAD v4: 9-116552014-C-T
• MyVariant Identifiers: chr9:g.119314293C>T (hg19) ; chr9:g.116552014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116552014C>T , CM000671.2:g.116552014C>T	GRCh38
NC_000009.11:g.119314293C>T , CM000671.1:g.119314293C>T	GRCh37
NC_000009.10:g.118354114C>T	NCBI36
NG_021409.1:g.868025G>A
NG_021409.2:g.868044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313400.9:c.3356-64514G>A (ASTN2) MANE Select	ENSP00000314038.4:n.3356-64514G>A
ENST00000361477.8:c.3203-64514G>A (ASTN2)	ENSP00000355116.5:n.3203-64514G>A
ENST00000288520.9:c.659-64514G>A (ASTN2)	ENSP00000288520.5:n.659-64514G>A
ENST00000313400.8:c.3356-64514G>A (ASTN2)	ENSP00000314038.4:n.3356-64514G>A
ENST00000341734.8:c.512-64514G>A (ASTN2)	ENSP00000339925.4:n.512-64514G>A
ENST00000361209.6:c.3203-64514G>A (ASTN2)	ENSP00000354504.2:n.3203-64514G>A
ENST00000361477.7:c.512-64514G>A (ASTN2)	ENSP00000355116.4:n.512-64514G>A
ENST00000373986.7:c.2525-64514G>A (ASTN2)	ENSP00000363098.3:n.2525-64514G>A
NM_001184734.1:c.512-64514G>A (ASTN2)	NP_001171663.1:n.512-64514G>A
NM_014010.4:c.3203-64514G>A (ASTN2)	NP_054729.3:n.3203-64514G>A
NM_198186.3:c.659-64514G>A (ASTN2)	NP_937829.3:n.659-64514G>A
NM_198187.3:c.512-64514G>A (ASTN2)	NP_937830.3:n.512-64514G>A
NM_198188.2:c.512-64514G>A (ASTN2)	NP_937831.1:n.512-64514G>A
NR_033973.1:n.1325-96C>T (ASTN2-AS1)
NM_001365068.1:c.3356-64514G>A (ASTN2) MANE Select	NP_001351997.1:n.3356-64514G>A
NM_001365069.1:c.3344-64514G>A (ASTN2)	NP_001351998.1:n.3344-64514G>A
NM_014010.5:c.3203-64514G>A (ASTN2)	NP_054729.3:n.3203-64514G>A