Canonical Allele Identifier: CA892654245

Gene: ZNF638

Linked Data

• dbSNP Id: rs1214375720
• gnomAD v3: 2-71381881-A-C
• gnomAD v4: 2-71381881-A-C
• MyVariant Identifiers: chr2:g.71609011A>C (hg19) ; chr2:g.71381881A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71381881A>C , CM000664.2:g.71381881A>C	GRCh38
NC_000002.11:g.71609011A>C , CM000664.1:g.71609011A>C	GRCh37
NC_000002.10:g.71462519A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264447.9:c.2377+1316A>C MANE Select	ENSP00000264447.4:n.2377+1316A>C
ENST00000264447.8:c.2377+1316A>C	ENSP00000264447.4:n.2377+1316A>C
ENST00000409544.5:c.2377+1316A>C	ENSP00000386433.1:n.2377+1316A>C
ENST00000410075.5:c.2377+1316A>C	ENSP00000485608.1:n.2377+1316A>C
ENST00000491843.2:n.224+978A>C
NM_001014972.2:c.2377+1316A>C	NP_001014972.1:n.2377+1316A>C
NM_001252612.1:c.2377+1316A>C	NP_001239541.1:n.2377+1316A>C
NM_001252613.1:c.2377+1316A>C	NP_001239542.1:n.2377+1316A>C
NM_014497.4:c.2377+1316A>C	NP_055312.2:n.2377+1316A>C
XM_005264263.1:c.844+1316A>C	XP_005264320.1:n.844+1316A>C
XM_006711989.1:c.844+1316A>C	XP_006712052.1:n.844+1316A>C
XM_011532767.1:c.2377+1316A>C	XP_011531069.1:n.2377+1316A>C
XM_011532768.1:c.2377+1316A>C	XP_011531070.1:n.2377+1316A>C
XM_011532769.1:c.2377+1316A>C	XP_011531071.1:n.2377+1316A>C
XR_939678.1:n.2492+1316A>C
XM_011532768.3:c.2695+1316A>C	XP_011531070.2:n.2695+1316A>C
XM_017003809.2:c.2695+1316A>C	XP_016859298.1:n.2695+1316A>C
XM_017003810.2:c.2377+1316A>C	XP_016859299.1:n.2377+1316A>C
XM_017003812.2:c.2695+1316A>C	XP_016859301.1:n.2695+1316A>C
XR_001738706.2:n.2741+1316A>C
XR_001738707.2:n.2679+1316A>C
XR_002959264.1:n.2741+1316A>C
XR_002959265.1:n.2741+1316A>C
XR_002959266.1:n.2741+1316A>C
XR_939678.3:n.2741+1316A>C
NM_014497.5:c.2377+1316A>C MANE Select	NP_055312.2:n.2377+1316A>C
NM_001014972.3:c.2377+1316A>C	NP_001014972.1:n.2377+1316A>C
NM_001252612.2:c.2377+1316A>C	NP_001239541.1:n.2377+1316A>C
NM_001252613.2:c.2377+1316A>C	NP_001239542.1:n.2377+1316A>C